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Serum Iron/Ibc

FDA UDI

by Sterling Diagnostics Inc

Identity

Trade Name
SERUM IRON/IBC FDA UDI
Generic Name
Iron IVD, reagent FDA UDI
Device Name
SERUM IRON/IBC COLORIMETRIC FDA UDI
Model / Reference
2200-0 FDA UDI
Description
SERUM IRON/IBC COLORIMETRIC FDA UDI

Identifiers

Catalog Number
2200-0 FDA UDI
Primary DI / UDI-DI
00852223007072 FDA UDI
GMDN Term
Iron IVD, reagent 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

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

Serum Iron/Ibc by Sterling Diagnostics Inc — 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 046feedf-a334-4a2a-99ca-289fd41a1752 34 fields · synced Jun 6, 2026