Identity
- Trade Name
- KaiBiLi Extended ViralTrans Saline FDA UDI
- Generic Name
- General specimen collection kit FDA UDI
- Device Name
- 1.2 mL vial with a small sterile swab FDA UDI
- Model / Reference
- M221129 FDA UDI
- Description
- 1.2 mL vial with a small sterile swab FDA UDI
Identifiers
- Primary DI / UDI-DI
- 16972698600569 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 Saline by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as General specimen collection kit.
- TUD NA CITRATE 0.109M 3ML — TUD SDN BHD · Class A
- GN Broth — Copan Italia S.P.A. · Class A
- Centurion — Centurion Medical Products · Class I
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class I
- LBM LIM Broth — Copan Italia S.P.A. · Class A
- BBL™ CultureSwab™ Plus — COPAN ITALIA SPA · Class I
- Transystem™ — COPAN ITALIA SPA · Class I
- UTM® — COPAN ITALIA SPA · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
Sources (1)
- FDA UDI 0a492966-387f-4bf6-9d46-c7bb6fc760ee 33 fields · synced May 30, 2026