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Iron Reagent Set

FDA UDI

Class I (US FDA UDI)

by Clinical Diagnostic Solutions, Inc.

Identity

Trade Name
Iron Reagent Set FDA UDI
Generic Name
Iron IVD, reagent FDA UDI
Device Name
For the quantitative determination of iron in serum. For in vitro diagnostic use only. FDA UDI
Model / Reference
R1 x 500mL, R2 x 15mL FDA UDI
Description
For the quantitative determination of iron in serum. For in vitro diagnostic use only. FDA UDI

Identifiers

Catalog Number
501-412 FDA UDI
Primary DI / UDI-DI
00812137011992 FDA UDI
FDA Product Code
JIY FDA UDI
GMDN Term
Iron IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1410 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

Yes

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

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: Iron IVD, reagent

Iron Reagent Set by Clinical Diagnostic Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Iron IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3836e05d-fb2e-4aba-9a99-420b89bdf5ef 36 fields · synced May 30, 2026