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Architect

FDA UDI

Class I (US FDA UDI)

by Abbott Laboratories, Inc.

Identity

Trade Name
ARCHITECT FDA UDI
Generic Name
Inorganic phosphate (PO43-) IVD, kit, spectrophotometry FDA UDI
Device Name
Phosphorus2 Conventional Units Assay Disk, Version 1.0 FDA UDI
Model / Reference
04T071A FDA UDI
Description
Phosphorus2 Conventional Units Assay Disk, Version 1.0 FDA UDI

Identifiers

Catalog Number
04T071A FDA UDI
Primary DI / UDI-DI
00380740191290 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Inorganic phosphate (PO43-) IVD, kit, spectrophotometry 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Inorganic phosphate (PO43-) IVD, kit, spectrophotometry

Architect by Abbott Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inorganic phosphate (PO43-) IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI be2fe73b-c7ad-4c8f-966f-dc147b3876d8 35 fields · synced May 30, 2026