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Vaginal PH Rapid Test Cassette

FDA UDI

Class I (US FDA UDI)

by Safecare Biotech (Hangzhou) Co., Ltd.

Identity

Trade Name
Vaginal PH Rapid Test Cassette FDA UDI
Generic Name
Vaginal pH screening IVD, kit, rapid colorimetric, clinical FDA UDI
Model / Reference
5 Tests FDA UDI

Identifiers

Catalog Number
PH-6012 FDA UDI
Primary DI / UDI-DI
06974246461342 FDA UDI
FDA Product Code
LNW FDA UDI
GMDN Term
Vaginal pH screening IVD, kit, rapid colorimetric, clinical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1550 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vaginal pH screening IVD, kit, rapid colorimetric, clinical

Vaginal PH Rapid Test Cassette by Safecare Biotech (Hangzhou) Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal pH screening IVD, kit, rapid colorimetric, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 07bef623-104c-4a78-87db-2a500eedb435 33 fields · synced May 30, 2026