← Back to catalogue

Pantex P631SC

FDA UDI

Class II (US FDA UDI)

by Pantex

Identity

Trade Name
Pantex P631SC FDA UDI
Generic Name
Total cortisol IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Salivary Cortisol EIA Control Level 1 FDA UDI
Model / Reference
P631SC FDA UDI
Description
Salivary Cortisol EIA Control Level 1 FDA UDI

Identifiers

Catalog Number
631 FDA UDI
Primary DI / UDI-DI
00850039602085 FDA UDI
FDA Product Code
NHG FDA UDI
GMDN Term
Total cortisol IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1205 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 cortisol IVD, kit, enzyme immunoassay (EIA)

Pantex P631SC by Pantex — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Pantex

Sources (1)

  • FDA UDI 83006afc-f328-4484-bb31-8719b0cb6aab 36 fields · synced May 30, 2026