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TGF Beta-1 ELISA

FDA UDI

Class I (US FDA UDI)

by American Laboratory Products Company

Identity

Trade Name
TGF Beta-1 ELISA FDA UDI
Generic Name
Human growth hormone (HGH) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
The TGF Beta-1 ELISA is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of TGF Beta-1 in serum and cell culture supernatant. For in vitro diagnostic use. FDA UDI
Model / Reference
20-TGF1HU-E01 FDA UDI
Description
The TGF Beta-1 ELISA is an enzyme immunoassay for the quantitative in vitro diagnostic measurement of TGF Beta-1 in serum and cell culture supernatant. For in vitro diagnostic use. FDA UDI

Identifiers

Catalog Number
20-TGF1HU-E01 FDA UDI
Primary DI / UDI-DI
B24220TGF1HUE010 FDA UDI
FDA Product Code
CFL FDA UDI
GMDN Term
Human growth hormone (HGH) IVD, kit, enzyme immunoassay (EIA) 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

No

FDA UDI

Category: Human growth hormone (HGH) IVD, kit, enzyme immunoassay (EIA)

TGF Beta-1 ELISA by American Laboratory Products Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Human growth hormone (HGH) IVD, kit, enzyme immunoassay (EIA).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d949d1e6-7f81-4326-8ca3-9b3116b5368e 36 fields · synced Jun 8, 2026