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Autostat II Anti-Thyroglobulin

FDA UDI

Class II (US FDA UDI)

by Hycor Biomedical Llc

Identity

Trade Name
Autostat II Anti-Thyroglobulin FDA UDI
Generic Name
Thyroglobulin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
96 well ELISA for the detection of Thyroglobulin antibodies in human serum FDA UDI
Model / Reference
FGA03 FDA UDI
Description
96 well ELISA for the detection of Thyroglobulin antibodies in human serum FDA UDI

Identifiers

Primary DI / UDI-DI
00816879020038 FDA UDI
FDA Product Code
DDC FDA UDI
GMDN Term
Thyroglobulin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5870 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-Thyroglobulin 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 18f6b690-9d6f-4a05-b81c-7bc68c64bb78 36 fields · synced May 30, 2026