← Back to catalogue

Lia Pregnancy Test

FDA UDI

Class II (US FDA UDI)

by Lia Diagnostics

Identity

Trade Name
Lia Pregnancy Test FDA UDI
Generic Name
Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, rapid agglutination, clinical FDA UDI
Model / Reference
2 Pack Discreet FDA UDI

Identifiers

Primary DI / UDI-DI
00860000380607 FDA UDI
FDA Product Code
LCX FDA UDI
GMDN Term
Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, rapid agglutination, 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, rapid agglutination, clinical

Lia Pregnancy Test by Lia Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, rapid agglutination, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Lia Diagnostics

Sources (1)

  • FDA UDI a763dc0b-a0bd-4b0f-aa03-7695d823549b 32 fields · synced May 30, 2026