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N Antiserum to Human a1-acid Glycoprotein

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
N Antiserum to Human a1-acid Glycoprotein FDA UDI
Generic Name
Alpha-1-acid glycoprotein (orosomucoid) IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Quantitative determination of a1-acid glycoprotein in human serum and plasma on BN Systems FDA UDI
Model / Reference
10446306 FDA UDI
Description
Quantitative determination of a1-acid glycoprotein in human serum and plasma on BN Systems FDA UDI

Identifiers

Catalog Number
OSAW09 FDA UDI
Primary DI / UDI-DI
00842768009877 FDA UDI
510(k) Number
K860894 FDA UDI
FDA Product Code
CFN FDA UDI
GMDN Term
Alpha-1-acid glycoprotein (orosomucoid) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5510 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

No

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

No

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

N Antiserum to Human a1-acid Glycoprotein by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID

Similar devices

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

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 a5971aee-fa3d-4032-be89-22d664a8d177 37 fields · synced May 31, 2026