Identity
- Trade Name
- KaiBiLi Extended ViralTrans PBS FDA UDI
- Generic Name
- General specimen collection kit FDA UDI
- Device Name
- Viral Transport,PBS 3 mL with Swab FDA UDI
- Model / Reference
- M221114 FDA UDI
- Description
- Viral Transport,PBS 3 mL with Swab FDA UDI
Identifiers
- Primary DI / UDI-DI
- 16972698600415 FDA UDI
- FDA Product Code
- JSG FDA UDI
- GMDN Term
- General specimen collection kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.2300 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General specimen collection kit
KaiBiLi Extended ViralTrans PBS by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
Sources (1)
- FDA UDI fce4441d-1b1d-4c51-bc33-3cd51421a4a3 33 fields · synced Jun 1, 2026