Identity
- Trade Name
- Reagent FDA UDI
- Generic Name
- Vitamin C (ascorbic acid) IVD, reagent FDA UDI
- Device Name
- Mobile Phase, Vitamin C in plasma/serum FDA UDI
- Model / Reference
- 65001 FDA UDI
- Description
- Mobile Phase, Vitamin C in plasma/serum FDA UDI
Identifiers
- Catalog Number
- 65001 FDA UDI
- Primary DI / UDI-DI
- 04250317513854 FDA UDI
- FDA Product Code
- JMA FDA UDI
- GMDN Term
- Vitamin C (ascorbic acid) IVD, reagent FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1095 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Vitamin C (ascorbic acid) IVD, reagent
Reagent by Chromsystems Instruments & Chemicals GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vitamin C (ascorbic acid) IVD, reagent.
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
- Chromsystems Instruments & Chemicals GmbH
Sources (1)
- FDA UDI d752a6c8-9abf-4b0d-a636-09e21509a335 37 fields · synced May 30, 2026