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Architect

FDA UDI

Class I (US FDA UDI)

by Abbott Laboratories, Inc.

Identity

Trade Name
ARCHITECT FDA UDI
Generic Name
Unsaturated iron binding capacity (UIBC) IVD, kit, spectrophotometry FDA UDI
Device Name
UIBC FDA UDI
Model / Reference
4R29-21 FDA UDI
Description
UIBC FDA UDI

Identifiers

Catalog Number
04R2921 FDA UDI
Primary DI / UDI-DI
00380740137045 FDA UDI
FDA Product Code
JQF FDA UDI
GMDN Term
Unsaturated iron binding capacity (UIBC) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1415 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: Unsaturated iron binding capacity (UIBC) 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 Unsaturated iron binding capacity (UIBC) IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Laboratories, Inc.

Sources (1)

  • FDA UDI d5f09824-e7bf-4ece-a364-5010236ea23f 36 fields · synced Jun 8, 2026