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Pantex P635ST

FDA UDI

Class I (US FDA UDI)

by Pantex

Identity

Trade Name
Pantex P635ST FDA UDI
Generic Name
Total testosterone IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Salivary Testosterone EIA Antibody FDA UDI
Model / Reference
P635ST FDA UDI
Description
Salivary Testosterone EIA Antibody FDA UDI

Identifiers

Catalog Number
635 FDA UDI
Primary DI / UDI-DI
00850039602238 FDA UDI
FDA Product Code
CDZ FDA UDI
GMDN Term
Total testosterone IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Category: Total testosterone IVD, kit, enzyme immunoassay (EIA)

Pantex P635ST by Pantex — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total testosterone IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pantex

Sources (1)

  • FDA UDI a3dded3a-b4c8-4fcd-960e-8b9780be1597 36 fields · synced May 30, 2026