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Anti-Tg AccuBind ELISA Test System - 96 Wells

FDA UDI

Class II (US FDA UDI)

by Monobind, Inc.

Identity

Trade Name
Anti-Tg AccuBind ELISA Test System - 96 Wells FDA UDI
Generic Name
Thyroglobulin antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
1025-300 FDA UDI

Identifiers

Catalog Number
1025-300A FDA UDI
Primary DI / UDI-DI
00816870020389 FDA UDI
510(k) Number
K971835 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
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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 7.75 Inch FDA UDI

Category: Thyroglobulin antibody IVD, kit, enzyme immunoassay (EIA)

Anti-Tg AccuBind ELISA Test System - 96 Wells by Monobind, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thyroglobulin antibody IVD, kit, enzyme immunoassay (EIA).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Monobind, Inc.

Sources (1)

  • FDA UDI b179c63a-764b-4bf7-9490-0d136933f951 37 fields · synced Jun 8, 2026