← Back to catalogue

Trichinella Antibody 96 Tests

FDA UDI

Class I (US FDA UDI)

by Scimedx Corp.

Identity

Trade Name
Trichinella Antibody 96 Tests FDA UDI
Generic Name
Trichinella spiralis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Model / Reference
TN-96 FDA UDI

Identifiers

Catalog Number
TN-96 FDA UDI
Primary DI / UDI-DI
00813545026493 FDA UDI
FDA Product Code
GPG FDA UDI
GMDN Term
Trichinella spiralis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3850 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Trichinella spiralis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Trichinella Antibody 96 Tests by Scimedx Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Trichinella spiralis immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA).

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

Manufacturer
Scimedx Corp.

Sources (1)

  • FDA UDI 79a4e6f3-a0ab-45b5-a7e2-c9ef20cdc1c8 34 fields · synced May 30, 2026