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Beta-Thal HbA2 Quik Column Kit

FDA UDI

Class II (US FDA UDI)

by Helena Laboratories, Corp.

Identity

Trade Name
Beta-Thal HbA2 Quik Column Kit FDA UDI
Generic Name
Inherited haemoglobinopathy IVD, reagent FDA UDI
Model / Reference
5341 FDA UDI

Identifiers

Primary DI / UDI-DI
M52553410 FDA UDI
FDA Product Code
JPD FDA UDI
GMDN Term
Inherited haemoglobinopathy IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.7400 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: Inherited haemoglobinopathy IVD, reagent

Beta-Thal HbA2 Quik Column Kit by Helena Laboratories, Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inherited haemoglobinopathy IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b357a772-66bf-41d1-b18c-70c0003bdb0c 33 fields · synced Jun 9, 2026