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Teco Diagnostics Vaginal pH Screening Kit

FDA UDI

Class I (US FDA UDI)

by Teco Diagnostics

Identity

Trade Name
Teco Diagnostics Vaginal pH Screening Kit FDA UDI
Generic Name
Vaginal pH screening IVD, kit, rapid colorimetric, self-testing FDA UDI
Device Name
Teco Diagnostics Vaginal pH Screening Kit is an easy, single-use device designed for testing pH in the vagina. FDA UDI
Model / Reference
MRS-OBGYN-VPH FDA UDI
Description
Teco Diagnostics Vaginal pH Screening Kit is an easy, single-use device designed for testing pH in the vagina. FDA UDI

Identifiers

Catalog Number
MRS-OBGYN-VPH FDA UDI
Primary DI / UDI-DI
10673486001037 FDA UDI
FDA Product Code
LNW FDA UDI
GMDN Term
Vaginal pH screening IVD, kit, rapid colorimetric, self-testing 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

Yes

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, self-testing

Teco Diagnostics Vaginal pH Screening Kit by Teco Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal pH screening IVD, kit, rapid colorimetric, self-testing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teco Diagnostics

Sources (1)

  • FDA UDI e6b1b4b4-0e27-4ea3-bc6d-b3fd578570a7 36 fields · synced May 30, 2026