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Trinity Biotech

FDA UDI

Class I (US FDA UDI)

by Mardx Diagnostics, Inc.

Identity

Trade Name
Trinity Biotech FDA UDI
Generic Name
Trypanosoma cruzi total antibody IVD, kit, fluorescent immunoassay FDA UDI
Device Name
Trypanosoma cruzi 6 Well Slide, 8 each pack FDA UDI
Model / Reference
20-03006 FDA UDI
Description
Trypanosoma cruzi 6 Well Slide, 8 each pack FDA UDI

Identifiers

Catalog Number
20-03006 FDA UDI
Primary DI / UDI-DI
05391516748865 FDA UDI
FDA Product Code
MIV FDA UDI
GMDN Term
Trypanosoma cruzi total antibody IVD, kit, fluorescent immunoassay FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3870 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

No

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: Trypanosoma cruzi total antibody IVD, kit, fluorescent immunoassay

Trinity Biotech by Mardx Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Trypanosoma cruzi total antibody IVD, kit, fluorescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 87a2faf8-69fe-441d-8aff-31aa0c54de17 36 fields · synced May 30, 2026