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HemoCue® Hb 201 Microcuvettes

FDA UDI

Class II (US FDA UDI)

by Hemocue, Inc.

Identity

Trade Name
HemoCue® Hb 201 Microcuvettes FDA UDI
Generic Name
Haemoglobin analyser IVD, point-of-care FDA UDI
Device Name
HemoCue Hb 201 Microcuvettes 4x50 vial FDA UDI
Model / Reference
111716 FDA UDI
Description
HemoCue Hb 201 Microcuvettes 4x50 vial FDA UDI

Identifiers

Catalog Number
111716 FDA UDI
Primary DI / UDI-DI
17311091117165 FDA UDI
510(k) Number
K032203 FDA UDI
FDA Product Code
GKR FDA UDI
GMDN Term
Haemoglobin analyser IVD, point-of-care 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

No

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: Haemoglobin analyser IVD, point-of-care

HemoCue® Hb 201 Microcuvettes by Hemocue, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemoglobin analyser IVD, point-of-care.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hemocue, Inc.

Sources (1)

  • FDA UDI 08c7135f-4d45-4faf-9bfd-87aefbdfff5d 36 fields · synced May 30, 2026