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A1 Acid Glycoprotein AMR Fluid

FDA UDI

Class I (US FDA UDI)

by The Binding Site Group

Identity

Trade Name
A1 Acid Glycoprotein AMR Fluid FDA UDI
Generic Name
Alpha-1-acid glycoprotein (orosomucoid) IVD, kit, nephelometry/turbidimetry FDA UDI
Model / Reference
BP527 FDA UDI

Identifiers

Primary DI / UDI-DI
05051700016667 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Alpha-1-acid glycoprotein (orosomucoid) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

No

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: Alpha-1-acid glycoprotein (orosomucoid) IVD, kit, nephelometry/turbidimetry

A1 Acid Glycoprotein AMR Fluid by The Binding Site Group — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alpha-1-acid glycoprotein (orosomucoid) IVD, kit, nephelometry/turbidimetry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ddbdf3ad-a362-45c7-b78f-abfea570ecfc 34 fields · synced Jun 8, 2026