Identity
- Trade Name
- ActivAT FDA UDI
- Generic Name
- Blood transfer set FDA UDI
- Device Name
- ActivAT Case of 8 Kits or 8 Trays with 966155500 ActivAT Outer Carton Label FDA UDI
- Model / Reference
- 966150000 FDA UDI
- Description
- ActivAT Case of 8 Kits or 8 Trays with 966155500 ActivAT Outer Carton Label FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10852714003009 FDA UDI
- GMDN Term
- Blood transfer set FDA UDI
Classification
- 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
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Category: Blood transfer set
ActivAT by Nuo Therapeutics, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Blood transfer set.
- SteriPath Gen2, 23G, BD — MAGNOLIA MEDICAL TECHNOLOGIES, INC. · Class II
- Accessories — OriGen Biomedical, Inc. · Class I
- Rem Systems — CODAN US Corporation · Class II
- Accessories — OriGen Biomedical, Inc. · Class I
- Trima Accel — Terumo BCT, Inc.. · Class II
- Spectra Optia® — Terumo BCT, Inc.. · Class II
- SteriPath Gen2, 21G, 10ml — MAGNOLIA MEDICAL TECHNOLOGIES, INC. · Class II
- Steripath Micro — MAGNOLIA MEDICAL TECHNOLOGIES, INC. · Class II
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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Nuo Therapeutics, Inc.
Sources (1)
- FDA UDI a06c0f35-ce0f-4f5d-8e29-8d1edcbebe34 33 fields · synced May 30, 2026