Identity
- Trade Name
- REMEL FDA UDI
- Generic Name
- Faecal specimen container IVD, fixative FDA UDI
- Device Name
- Cary-Blair w/Ind/SAF PK/6SET FDA UDI
- Model / Reference
- R21615 FDA UDI
- Description
- Cary-Blair w/Ind/SAF PK/6SET FDA UDI
Identifiers
- Catalog Number
- R21615 FDA UDI
- Primary DI / UDI-DI
- 00848838023972 FDA UDI
- 510(k) Number
- K013711 FDA UDI
- FDA Product Code
- LIO FDA UDI
- GMDN Term
- Faecal specimen container IVD, fixative FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.2900 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Faecal specimen container IVD, fixative
Remel by Remel, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K013711 also covers:
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
- Manufacturer
- Remel, Inc.
Sources (1)
- FDA UDI a4ea1c3d-ed80-49a4-a501-8720c28ec891 35 fields · synced May 30, 2026