Identity
- Trade Name
- FENTEX FDA UDI
- Generic Name
- Medicine bottle FDA UDI
- Device Name
- Spare Bottle brown, for 832600FX 30 cc FDA UDI
- Model / Reference
- 832601FX FDA UDI
- Description
- Spare Bottle brown, for 832600FX 30 cc FDA UDI
Identifiers
- Catalog Number
- 832601FX FDA UDI
- Primary DI / UDI-DI
- 04250407754501 FDA UDI
- FDA Product Code
- LRC FDA UDI
- GMDN Term
- Medicine bottle FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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: Medicine bottle
Fentex by FENTEX medical GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Medicine bottle.
- ChemoPlus — Cardinal Health 200, LLC · Class II
- ChemoPlus — Cardinalhealth · Class II
- ChemoPlus — Cardinalhealth · Class II
- ChemoPlus — Cardinalhealth · Class II
- ChemoPlus — Cardinalhealth · Class II
- ChemoPlus — Cardinal Health 200, LLC · Class II
- Safer Lock — Rxguardian Inc. · Class I
- ChemoPlus — Cardinalhealth · 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 | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- FENTEX medical GmbH
Sources (1)
- FDA UDI eb94e332-f70c-4f8f-8cff-510c1c3d9448 35 fields · synced May 30, 2026