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hemochroma PLUS Starter Kit

FDA UDI

Class II (US FDA UDI)

by Immunostics, Inc.

Identity

Trade Name
hemochroma PLUS Starter Kit FDA UDI
Generic Name
Total haemoglobin (totHb) IVD, kit, spectrophotometry FDA UDI
Device Name
1 hemochroma PLUS Analyzer+100 Microcuvettes+1 optical system check FDA UDI
Model / Reference
100-PROMO FDA UDI
Description
1 hemochroma PLUS Analyzer+100 Microcuvettes+1 optical system check FDA UDI

Identifiers

Catalog Number
100-PROMO FDA UDI
Primary DI / UDI-DI
10722355003051 FDA UDI
FDA Product Code
GKR FDA UDI
GMDN Term
Total haemoglobin (totHb) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5620 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Total haemoglobin (totHb) IVD, controlTotal haemoglobin (totHb) IVD, kit, spectrophotometryTotal haemoglobin (totHb) IVD, reagent

hemochroma PLUS Starter Kit by Immunostics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total haemoglobin (totHb) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Immunostics, Inc.

Sources (1)

  • FDA UDI acefab10-66ff-4fc6-89f5-5b6d1300d575 36 fields · synced May 30, 2026