← Back to catalogue

Optilite® α1-Acid Glycoprotein Control Pack

FDA UDI

Class I (US FDA UDI)

by The Binding Site Group

Identity

Trade Name
Optilite® α1-Acid Glycoprotein Control Pack FDA UDI
Generic Name
Alpha-1-acid glycoprotein (orosomucoid) IVD, control FDA UDI
Model / Reference
NQ063.OPT FDA UDI

Identifiers

Primary DI / UDI-DI
05051700019002 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Alpha-1-acid glycoprotein (orosomucoid) IVD, control 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

Yes

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, control

Optilite® α1-Acid Glycoprotein Control Pack by The Binding Site Group — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 563656c6-5122-44a5-be1e-492f4ad60809 34 fields · synced Jun 6, 2026