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Tgf-B2 Elisa

FDA UDI

Class I (US FDA UDI)

by DRG International, Inc.

Identity

Trade Name
TGF-B2 ELISA FDA UDI
Generic Name
Trypanosoma brucei total antibody IVD, kit, rapid ICT, clinical FDA UDI
Device Name
The DRG TGF-ß2 ELISA is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of TGF-ß2 in serum, plasma and cell culture supernatant. FDA UDI
Model / Reference
EIA-2396 FDA UDI
Description
The DRG TGF-ß2 ELISA is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of TGF-ß2 in serum, plasma and cell culture supernatant. FDA UDI

Identifiers

Catalog Number
EIA-2396 FDA UDI
Primary DI / UDI-DI
00840239023964 FDA UDI
FDA Product Code
CFL FDA UDI
GMDN Term
Trypanosoma brucei total antibody IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1370 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Trypanosoma brucei total antibody IVD, kit, rapid ICT, clinical

Tgf-B2 Elisa by DRG International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d0e2dec-2007-4cc6-a4c2-ffc9b6b2ded1 36 fields · synced May 30, 2026