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Hemoglobin Control Solution

FDA UDIEUDAMED

Class II (US FDA UDI)

by Urit Medical Electronic Co., Ltd.

Identity

Trade Name
Hemoglobin Control Solution FDA UDI
Generic Name
Haemoglobin detection IVD, control FDA UDI
Model / Reference
HQ-A,1mL/bottle×3/box FDA UDI

Identifiers

Primary DI / UDI-DI
06935740733854 FDA UDI
FDA Product Code
GGM FDA UDI
GMDN Term
Haemoglobin detection IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.8625 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Haemoglobin detection IVD, control

Hemoglobin Control Solution by Urit Medical Electronic Co., Ltd. — Class II — IVDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Haemoglobin detection IVD, control.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI bd3acfdb-39b4-4439-9e9f-a5e6d0ba70b7 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 18, 2026