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Research and Diagnostic Systems

FDA UDI

Class II (US FDA UDI)

by Research And Diagnostic Systems, Inc.

Identity

Trade Name
Research and Diagnostic Systems FDA UDI
Generic Name
Multiple form 25-hydroxy Vitamin D IVD, reagent FDA UDI
Device Name
Human Total 25-OH Vitamin D IVD ELISA Kit FDA UDI
Model / Reference
RDKAP1971 FDA UDI
Description
Human Total 25-OH Vitamin D IVD ELISA Kit FDA UDI

Identifiers

Catalog Number
RDKAP1971 FDA UDI
Primary DI / UDI-DI
00815762021718 FDA UDI
FDA Product Code
MRG FDA UDI
GMDN Term
Multiple form 25-hydroxy Vitamin D IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1825 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: Multiple form 25-hydroxy Vitamin D IVD, reagent

Research and Diagnostic Systems by Research And Diagnostic Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple form 25-hydroxy Vitamin D IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b4883cdc-2959-4e70-ac0f-10e312171033 36 fields · synced Jun 1, 2026