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Autostat II Anti-GBM

FDA UDI

Class II (US FDA UDI)

by Hycor Biomedical Llc

Identity

Trade Name
Autostat II Anti-GBM FDA UDI
Generic Name
Glomerular basement membrane antibody (Goodpasture antibody) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
96 well ELISA for the detection of anti-GBM antibodies in human serum FDA UDI
Model / Reference
FGA13 FDA UDI
Description
96 well ELISA for the detection of anti-GBM antibodies in human serum FDA UDI

Identifiers

Primary DI / UDI-DI
00816879020137 FDA UDI
FDA Product Code
MVJ FDA UDI
GMDN Term
Glomerular basement membrane antibody (Goodpasture antibody) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5660 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Autostat II Anti-GBM by Hycor Biomedical Llc — Class II — 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 ce246b9b-ed4a-430d-86a8-9a9276f5c463 36 fields · synced May 30, 2026