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Rite Aid

FDA UDI

Class II (US FDA UDI)

by Guangzhou Decheng Biotechnology Co., LTD

Identity

Trade Name
Rite Aid FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Rite Aid Pregnancy Tests, 1 Digital Pregnancy Rapid Test + 1 Early Detection Pregnancy Test, combo test kit FDA UDI
Model / Reference
2T FDA UDI
Description
Rite Aid Pregnancy Tests, 1 Digital Pregnancy Rapid Test + 1 Early Detection Pregnancy Test, combo test kit FDA UDI

Identifiers

Primary DI / UDI-DI
00011822024419 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

Yes

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

Yes

FDA UDI

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

Rite Aid by Guangzhou Decheng Biotechnology Co., LTD — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8dfa2a40-f81e-4e3c-a8ce-ad0e05ef62a7 33 fields · synced May 30, 2026