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Architect

FDA UDI

Class I (US FDA UDI)

by Abbott Ireland Diagnostics

Identity

Trade Name
ARCHITECT FDA UDI
Generic Name
Chemiluminescent immunoassay signal generation kit IVD FDA UDI
Device Name
ARCHITECT TRIGGER SOLUTION FDA UDI
Model / Reference
6C55-60 FDA UDI
Description
ARCHITECT TRIGGER SOLUTION FDA UDI

Identifiers

Catalog Number
06C5560 FDA UDI
Primary DI / UDI-DI
00380740009625 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Chemiluminescent immunoassay signal generation kit IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 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

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: Chemiluminescent immunoassay signal generation kit IVD

Architect by Abbott Ireland Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chemiluminescent immunoassay signal generation kit IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b83d41da-489c-4ea2-981c-1a5a40cd4b83 36 fields · synced May 30, 2026