Identity
- Trade Name
- Tri-Tech Forensics, Inc. FDA UDI
- Generic Name
- Non-evacuated blood collection tube IVD, potassium oxalate/sodium fluoride FDA UDI
- Device Name
- 10 ml Grey Stoppered Blood Tube, Each FDA UDI
- Model / Reference
- TUG10 FDA UDI
- Description
- 10 ml Grey Stoppered Blood Tube, Each FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00869373000204 FDA UDI
- 510(k) Number
- K971111 FDA UDI
- FDA Product Code
- JKA FDA UDI
- GMDN Term
- Non-evacuated blood collection tube IVD, potassium oxalate/sodium fluoride FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1675 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
Dimensions & Sizes
- Size
- Total Volume — 10 Milliliter FDA UDI
Category: Non-evacuated blood collection tube IVD, potassium oxalate/sodium fluoride
Tri-Tech Forensics, Inc. by Tri-Tech Forensics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- Tri-Tech Forensics Inc.
Sources (1)
- FDA UDI f9a214d2-680a-4615-b25a-56eea74e0ebe 35 fields · synced May 30, 2026