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Gynex

FDA UDI

Class I (US FDA UDI)

by Gynex Corporation

Identity

Trade Name
Gynex FDA UDI
Generic Name
Vaginal pH screening IVD, kit, rapid colorimetric, clinical FDA UDI
Model / Reference
PH-99 FDA UDI

Identifiers

Primary DI / UDI-DI
GYNXPH991 FDA UDI
510(k) Number
K032161 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Gynex by Gynex Corporation — 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

Manufacturer
Gynex Corporation

Sources (1)

  • FDA UDI 15c1d55a-3b98-4315-a7d9-ae9d1e161dd0 33 fields · synced May 31, 2026