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HCG Home Use Pregnancy Test Midstream (Colloidal Gold)

FDA UDI

Class II (US FDA UDI)

by Anhui Deepblue Medical Technology Co., Ltd

Identity

Trade Name
HCG Home Use Pregnancy Test Midstream (Colloidal Gold) FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
Device Name
The HCG Home Use Pregnancy Test Midstream (Colloidal Gold) is a rapid chromatographic immunoassay for thequalitative detection of human chorionic gonadotropin (hCG) in urine to aid in the early detection of pregnancy. FDA UDI
Model / Reference
Midstream,5PCS/BOX FDA UDI
Description
The HCG Home Use Pregnancy Test Midstream (Colloidal Gold) is a rapid chromatographic immunoassay for thequalitative detection of human chorionic gonadotropin (hCG) in urine to aid in the early detection of pregnancy. FDA UDI

Identifiers

Primary DI / UDI-DI
06952062778165 FDA UDI
510(k) Number
K240242 FDA UDI
FDA Product Code
JHI 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

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

Yes

FDA UDI

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

HCG Home Use Pregnancy Test Midstream (Colloidal Gold) by Anhui Deepblue Medical Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID

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 50eff537-ef2a-4544-8c4f-a313167b9ebc 34 fields · synced Jun 8, 2026