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Triage

FDA UDI

Class I (US FDA UDI)

by Quidel Cardiovascular Inc.

Identity

Trade Name
Triage FDA UDI
Generic Name
Multiple cardiac marker IVD, control FDA UDI
Device Name
Quidel Triage Total 3 Control 1 FDA UDI
Model / Reference
88733 FDA UDI
Description
Quidel Triage Total 3 Control 1 FDA UDI

Identifiers

Catalog Number
88733 FDA UDI
Primary DI / UDI-DI
30014613337089 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Multiple cardiac marker IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Multiple cardiac marker IVD, control

Triage by Quidel Cardiovascular Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple cardiac marker IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b85831f8-9ad3-4dd0-af6b-bce3a559d77a 35 fields · synced May 31, 2026