Application:
HV test shielding room (faraday cage) are Widely used in power cable, transformer, transformer switch, transformer substation and other High voltage levels of partial discharge test or impulse test.
For HV testing shielding room, as a HV test place, it should has good electromagnetic
shielding condition. And its electromagnetic compatibility always is of great importance.
Firstly, it should restrict electromagnetic wave into inside shielding room caused by
discharge when making HV test to weakening interfere to outside, especially on
electronic and communication system. Secondly, it should prevent outer
electromagnetic wave intruding into shielding room to cause measurement error of
partial discharge and wireless. Thirdly, it should reduces open circuit voltage and
closed current to restrain common-mode interference so that to avoid equipment
damage and to improve accuracy of impulse measurement.
For GIS HV test shielding room, design area is 500 m2ï¼?Length 25mã??Width 20m).
From provided information , we find that steel structure have been completed
already with one set of 20T crane indoor, crane supporting corbel also completed, the
height is 17.9m from ground to upper part of corbel. Main door height 13m,width 10m,
locates at downward of the west side, the door open direction towards to north .
According to ILJIN drawing, three side of structure column has already, but western
structure column still missing yet. however, as the main door will be located in this side,
the western side also should have steel structure , and this structure position still should
be unified considered with main door installation. We will be able to submit suggested
design diagram with position & size of this structure column for reference. in order to
save construction cost, the construction engineering will be carried out by ILJIN
team.
4.Excellent Anti-corrosive And Excellent Weather Resistance.
PVC roof tile can long resist acid, alkali, salt and other corrosive chemicals. It suitable for using in corrosive workshop, acid rain-prone area and coastal area.
5.Good Fire Resistance With Excellent Insulation And Excellent Waterproof Performance.
Belonging flame retardant material, with fire resistance tested by national authoritative departments. The roofing sheet selects highly weather-resistant resin, which is dense and
absorbing no water, with no pore penetration problem.
Application:
HV test shielding room (faraday cage) are Widely used in power cable, transformer, transformer switch, transformer substation and other High voltage levels of partial discharge test or impulse test.
Due to increased environmental electromagnetic pollution, sensitive and accurate measurements are often affected by RF noise. The application of CNME Intermational Shielding Room provide the highest possible shielding attenuation, creating a controlled electromagnetic environment to perform high sensitive testing without distortion. If you are interested in our Faraday Cage, you can call us now.
ECG cables also referred to as an ECG patient cable, is a type of cable connection designed for non-invasive heart monitoring, typically used to help diagnose potential heart issues. The ECG cable connects to electrodes which are positioned at specific locations on the patient�¢??s body to detect and record heart muscle electrical activity. The cables then transmit the electrical activity back to the ECG device for analysis and diagnosis by medical professionals.
ECG Cable Feature
[Multiple Leads]: ECG cables usually have several leads placed in specific areas on the patient�¢??s body, such as the chest, arms, and legs, to measure the heart�¢??s electrical activity from different angles.
[Durability]: ECG cables are constructed from top-quality, sturdy materials that can endure repeated bending, tugging, and
twisting without sustaining any damage. This ensures that the cables can withstand the rigors of frequent use and remain reliable over time.
[Shielding]: ECG cables are shielded to block out external electrical signals, which can interfere with the accuracy of the
readings.
[Connector Compatibility]: The ECG cables are available with various connector types, including snap, clip, and banana, to fit different types of ECG machines.
[Safety]: ECG cables are designed to meet strict safety standards and regulations to ensure patient safety. This helps to ensure that patients are protected from any potential harm during the monitoring process.
[Cleaning and Disinfecting]: The ECG cables are easy to clean and disinfect to maintain hygienic conditions, as they come into contact with the patient�¢??s skin.
ECG Cable Advantages
[Excellent Performance]: ECG cables are built to withstand the rigors of twisting and bending, and have been thoroughly tested to ensure optimal performance. The cables are also equipped with electrical shielding to protect the signal integrity, ensuring accurate readings.
[Non-Invasive]: ECG cables are non-invasive, which means that they do not require any incisions or invasive procedures. This reduces the risk of infection and makes the monitoring process much safer for patients. Instead, the cables are simply attached to the patient's skin, making it a quick and painless process.
Application
Use for control and connecting cable on data transmission within building management system, speaker audio system and control measurement. Suitable for use in dry and damp environment.
Cable Structure & Features
Conductor Material : Tinned copper stranded
Insulation : Semi-Rigid PVC
Drain Wire : Tinned copper stranded
Shielding : Aluminium foil laminated screen
Outer Sheath ; PVC
Sheath Colour : black or gray
Technical Data
Standard : UL Style 2464
Approvals : UL apporoved
Rated Voltage : 300V
Testing Voltage : 1500V
Flame Retardant : VW-1
Insulation Resistance : Min 20Mx km
Min. Bending Radius : 10 x cable diameter
Operating Temp. : -30C / +80C
1929 Shielding Hall Of Hv Pd Test Suppliers
Short on time? Let Shielding Hall Of Hv Pd Test sellers contact you.
Double sided anti fog face shield
Anti Spray, anti dust, anti fume, high definition perspective can b disinfected and reused Product size thickness 0.2, length 320m, height 220 , belt 683mm, product weight -29.5 g
Double sided anti fog face shield
Anti Spray, anti dust, anti fume, high definition perspective can b disinfected and reused Product size thickness 0.2, length 320m, height 220 , belt 683mm, product weight -29.5 g
meppys 36g medical FACE SHIELD
PROTECTION VISOR
Model charateristics:
CE certification: EN166.-3
FIlm material: polycarbonate 0,38mm film
Frame colour: clear (transparent) with blue or green tabs
Packing: bulk or single
USP: suitable for medical environments
MOQ: 100 pcs
Long awaited, now the time has come: meppys is now also available as a protective face shield for the medical sector! meppys 36g medical is characterized by a stronger, more resistant special film made of 0.38mm thick polycarbonate. Its suitability for the medical purposes has been confirmed by extensive tests, therefore the product is CE EN 166-3 compliant. And just like our other products, this face visor can be used by glass-wearers.
Face shield PRICE/PC CIF Major ports worldwide
USD1.10/pc
It consists of a protective cover, foam strip and fixing device made of polymer materials.
2. Nonsterile, single-use.
3. Anti-fog
CE/FDA certificates
200/CTN
67.5X44X36 CM 0.1 CBM/CTN
600 ctns, 120,000 pcs / 40'HQ container
280 ctns 56000 pcs in 1x20 container
Coverage: Foreheads, Eyes, Nose, Mouth & Neck
Protection: Spattering from an infected individual
Scratch Resistant Special UV Printing with Food Grade Inks
Made from PET (Polyethylene Terephthalate)
Front Sheet Size: 280 X 208 mm
Foam Density 32, Foam Size 1 Inch & 1 Inch Elastic
Available in Many Design as per Catalogue
ISO & CE Approved
Tested in accodance to MoEF Recognised Govt. Approved Test House
Pet Sheet Thickness 250, 400, 550, 2000 Micron
Light Weight
Comfortable & No Breathing Issue
ISO Approved
Sample Types :
Including Nasopharyngeal swab, Oropharyngeal swab, Sputum
Controls :
Internal control, UNG enzyme and dUTP used to reduce risk of contamination, false positive and false negative results
Product Information
Upper and lower respiratory specimens such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate.
Authorized Laboratories
Laboratories certified under the Clinical Laboratory Improvement Amendments
of 1988 (CLIA), 42 U.S.C. 263a, to perform high complexity tests.
About Emergency Use Authorization
(EUA)
This test (1) has not been FDA cleared or approved, (2) has been authorized by
FDA under an EUA for use by authorized laboratories, (3) has been authorized
only for the detection of nucleic acid from SARS-CoV-2, not for any other
viruses or pathogens, and (4) is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C.360bbb-3(b)(1), unless the authorization
is terminated or revoked sooner.
The COVID-19 RT-PCR Detection Kit is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in upper and lower respiratory specimens (such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal
aspirate) from individuals suspected of COVID-19 by their healthcare provider. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments (CLIA) of 1988, 42 U.S.C.
263a, to perform high complexity tests.
Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in upper and lower respiratory specimens during the acute phase of infection. Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infective status. The agent detected may not be
the definite cause of disease. Positive results do not rule out bacterial co-infection with other viruses.
Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities.
Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations, patient history, and epidemiological information.
The COVID-19 RT-PCR Detection Kit is intended for use by qualified trained clinical laboratory personnel specifically instructed and trained in the techniques of real-time PCR and in vitro diagnostic procedures. The COVID-19 RT-PCR Detection Kit is only for use under the Food and Drug Administration's Emergency Use Authorization.
PRINCIPLE OF DETECTION
This product is a fluorescent probe-based Taqman RT-PCR assay system. Firstly, the RNA of SARS-CoV-2 will be reverse transcribed into cDNA by reverse transcriptase, and then PCR amplification will be performed with cDNA as template. During amplification of the template, the TaqMan probe will
be degraded due to the 5'-3 polymerase activity and exonuclease activity of Taq DNA polymerase, then the separation of fluorescent reporter and quencher enables the fluorescent signal to be detected by instrument. The ORF1ab gene of SARS-CoV-2 will be detected qualitatively by FAM channel, the N
gene of SARS-CoV-2 will be detected qualitatively by JOE channel, the E gene of SARS-CoV-2 will be detected qualitatively by ROX channel, and the internal reference will be detected by CY5 channel.
dUTP and UNG enzyme are used in the kit to prevent contamination of the amplified products.
Internal reference is used in the kit for quality control starting from sample collection
Indication: Qualitative detection of nucleic acid from SARS-CoV-2 in upper
and lower respiratory specimens (such as anterior nasal swabs, mid-turbinate nasal swabs, nasopharyngeal swabs, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate) from individuals suspected of COVID-19 by their healthcare provider.
Emergency use of this test is limited to authorized laboratories.
Authorized Laboratories: Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform high
complexity tests.
This letter is in response to your1 request that the Food and Drug Administration (FDA) issue an Emergency Use Authorization (EUA) for emergency use of your product,2 pursuant to Section 564 of the Federal Food, Drug, and Cosmetic Act (the Act) (21 U.S.C. 360bbb-3). On February 4, 2020, pursuant to Section 564(b)(1)(C) of the Act, the Secretary of the
Department of Health and Human Services (HHS) determined that there is a public health emergency that has a significant potential to affect national security or the health and security of United States citizens living abroad, and that involves the virus that causes COVID-19.
Pursuant to Section 564 of the Act, and on the basis of such determination, the Secretary of HHS then declared that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of the virus that causes COVID-19 subject to the terms of any authorization issued under Section 564(a) of the Act.
Having concluded that the criteria for issuance of this authorization under Section 564(c) of the Act are met, I am authorizing the emergency use of your product, described in the Scope of Authorization of this letter (Section II), subject to the terms of this authorization.
I. Criteria for Issuance of Authorization I have concluded that the emergency use of your product meets the criteria for issuance of an authorization under Section 564(c) of the Act, because I have concluded that:
1. The SARS-CoV-2 can cause a serious or life-threatening disease or condition,
including severe respiratory illness, to humans infected by this virus;
2. Based on the totality of scientific evidence available to FDA, it is reasonable to believe that your product may be effective in diagnosing COVID-19, and that the known and potential benefits of your product when used for diagnosing COVID-19, outweigh the known and potential risks of your product; and, 3. There is no adequate, approved, and available alternative to the emergency use of your
product.
4
II. Scope of Authorization
I have concluded, pursuant to Section 564(d)(1) of the Act, that the scope of this authorization is limited to the indication above.
Commodity: Covid-19 RT-PCR Detection Kit
Spec.96 tests/kit
Price:FOB SHANGHAI USD3.30/test, USD316.8/kit
$3.60/TEST CIF NY AIRPORT OR OTHER MAJOR AIRPORTS USA OR EUROPE OR S. AMERICA OR MIDDLE EAST
Payment: T/T ADVANCE 50% BALANCE BEFORE DEPARTURE OR Sight Irrevocable TRANSFERABLE LC Delivery: By AIR, 50days after receipt and confirmation of LC
Dimensions are 320mm x 220mm x 0.5mm thick. The shield is double side anti-fog and the headband is made of food-grade PDA approved polypropylene resin. The shield has TPE adjustable strap to accommodate various head sizes. The shield is re-useable and made of product which can be sterilized using disinfecting wipes or a reduced bleach solution. Designed for comfort and the ability to be work for 8+ hour shifts. This product is well and and will last. The price is for a box with 200 shields including instructions.
- FDA Approved
- This full face Cap made of highly transparent and environmentally friendly PET material.
- Comfortable to wear.
- Comprehensive protection, double sided, it can effectively protect your entire face from spitting, dust, water.
- The face Cap is lightweight, making it great for travel and storage.
- Suitable for outdoor and home, for daily protection, anti-fog, anti-spitting, anti-oil splash, etc.
- Transparent design, wide view.
- It's a useful gift for your friends and families.
Note:
1. Due to the light and screen difference, the item color may be slightly different from the pictures.
2. Please allow 1-2 cm differences due to manual measurement.
Protects face and eyes from flying debris and hazardous chemicals
Anti-fog function provides clear vision.
Easy to adjust for a custom secure fit, with elastic headband.
REUSABLE FACE SHIELD
Spec as follows;
- Material: new Pet, 2-3 zem
- Anti-fog
- Color: white
- Elastic band: 320*20mm
- Sponge: 250*30*25mm
- Level 3:
-CERTIFICATES â?? STANDARDS
FDA Facility Registration
ISO 13485
Test report: ANSI/AAMI PB70
CE marking, FDA
FDA, CE, ISO APPROVED.
Application: Health division and disease control
Quantity: (5 Million Pieces)
Packaging Instruction: 200 pcs /carton
Full order shipment expected to complete in less than 6 months Max. (Partial Shipments Allowed)
