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Salivary Testosterone ELISA

FDA UDI

Class I (US FDA UDI)

by DRG International, Inc.

Identity

Trade Name
Salivary Testosterone ELISA FDA UDI
Generic Name
Total testosterone IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The Salivary Testosterone ELISA is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of free active testosterone in saliva. FDA UDI
Model / Reference
SLV-3013 FDA UDI
Description
The Salivary Testosterone ELISA is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of free active testosterone in saliva. FDA UDI

Identifiers

Catalog Number
SLV-303 FDA UDI
Primary DI / UDI-DI
00840239030139 FDA UDI
510(k) Number
K052649 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

Yes

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

Yes

FDA UDI

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

Salivary Testosterone ELISA by DRG International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ad7c1d96-a7a0-4db9-bde2-d388c43650f1 37 fields · synced Jun 8, 2026