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Pantex Universal

FDA UDI

Class I (US FDA UDI)

by Pantex

Identity

Trade Name
Pantex Universal FDA UDI
Generic Name
Total testosterone IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Stopping Solution EIA 1 - 15mL FDA UDI
Model / Reference
1 Universal FDA UDI
Description
Stopping Solution EIA 1 - 15mL FDA UDI

Identifiers

Catalog Number
635 FDA UDI
Primary DI / UDI-DI
00850039602276 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 Universal 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 b193396d-7ef4-460d-8b22-1d63e9fee10a 36 fields · synced Jun 8, 2026