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Vitamin D Control

FDA UDI

Class I (US FDA UDI)

by Fujirebio Diagnostics, Inc.

Identity

Trade Name
Vitamin D Control FDA UDI
Generic Name
25-Hydroxy vitamin D3 IVD, control FDA UDI
Model / Reference
2130152 FDA UDI

Identifiers

Primary DI / UDI-DI
00850212007034 FDA UDI
510(k) Number
K110641 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
25-Hydroxy vitamin D3 IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: 25-Hydroxy vitamin D3 IVD, control

Vitamin D Control by Fujirebio Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as 25-Hydroxy vitamin D3 IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fujirebio Diagnostics, Inc.

Sources (1)

  • FDA UDI 4f1210e0-ce3c-4857-83fa-3c8a955768ed 36 fields · synced Jun 9, 2026