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Alltest hCG Early Pregnancy Rapid Test

FDA UDIEUDAMED

Class II (US FDA UDI)

by Hangzhou AllTest Biotech Co., Ltd.

Identity

Trade Name
Alltest hCG Early Pregnancy Rapid Test FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
Device Name
1T, FDA OTC FDA UDI
Model / Reference
1 FDA UDI
Description
1T, FDA OTC FDA UDI

Identifiers

Primary DI / UDI-DI
06936983155748 FDA UDI
FDA Product Code
LCX FDA UDI
GMDN Term
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1155 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

Yes

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: Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

Alltest hCG Early Pregnancy Rapid Test by Hangzhou AllTest Biotech Co., Ltd. — Class II — IVDD, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical.

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 f489498c-7cf1-48b8-a7ba-c8a73aebe446 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 18, 2026