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Alpha-1-Acid-Glycoprotein (agt)

FDA UDI

Class I (US FDA UDI)

by Randox Laboratories, Ltd.

Identity

Trade Name
ALPHA-1-ACID-GLYCOPROTEIN (AGT) FDA UDI
Generic Name
Alpha-1-acid glycoprotein (orosomucoid) IVD, kit, nephelometry/turbidimetry FDA UDI
Model / Reference
AG2472 FDA UDI

Identifiers

Primary DI / UDI-DI
05055273200126 FDA UDI
FDA Product Code
LKL FDA UDI
GMDN Term
Alpha-1-acid glycoprotein (orosomucoid) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.5420 FDA UDI
Commercial Distribution
Not 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

No

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

Alpha-1-Acid-Glycoprotein (agt) by Randox Laboratories, Ltd. — 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 f1f53edb-f36b-4b95-b2b9-5704a4c7c069 34 fields · synced May 30, 2026