Identity
- Trade Name
- Vitamin D FDA UDI
- Generic Name
- Multiple form 25-hydroxy Vitamin D IVD, control FDA UDI
- Device Name
- Vitamin D FDA UDI
- Model / Reference
- 83638 FDA UDI
- Description
- Vitamin D FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817238011551 FDA UDI
- GMDN Term
- Multiple form 25-hydroxy Vitamin D IVD, control FDA UDI
Classification
- 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
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
No
FDA UDI
Category: Multiple form 25-hydroxy Vitamin D IVD, control
Vitamin D by Cliniqa Corporation — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- BioPlex 2200 — Bio-Rad Laboratories · Class I
- Method Verification Kit - Vitamin D — QUALIGEN INC. · Class I
- Atellica IM VitD MCM — Siemens Healthcare Diagnostics · Class I
- Diazyme — Diazyme Laboratories, Inc.
- Alinity — ABBOTT IRELAND · Class I
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 |
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Manufacturer
- Manufacturer
- Cliniqa Corporation
Sources (1)
- FDA UDI 16635983-a20d-4729-a31f-f2e693265d6d 33 fields · synced May 30, 2026