Identity
- Trade Name
- Millennium FDA UDI
- Generic Name
- Transforming growth factor beta protein IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- Perfusion Tubing Organizer Standard 6 Slots FDA UDI
- Model / Reference
- 1-PTOS FDA UDI
- Description
- Perfusion Tubing Organizer Standard 6 Slots FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00190776307684 FDA UDI
- FDA Product Code
- KRI FDA UDI
- GMDN Term
- Transforming growth factor beta protein IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.4200 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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Transforming growth factor beta protein IVD, kit, enzyme immunoassay (EIA)
Millennium by AVALIGN TECHNOLOGIES, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Transforming growth factor beta protein IVD, kit, enzyme immunoassay (EIA).
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
- AVALIGN TECHNOLOGIES, Inc.
Sources (1)
- FDA UDI 27ddf771-de01-4a60-89b8-8a692c23cad9 34 fields · synced Jun 8, 2026