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Architect

FDA UDI

Class I (US FDA UDI)

by Abbott Laboratories, Inc.

Identity

Trade Name
ARCHITECT FDA UDI
Generic Name
Lipoprotein A IVD, calibrator FDA UDI
Device Name
Lp(a) Calibrators FDA UDI
Model / Reference
5P83-01 FDA UDI
Description
Lp(a) Calibrators FDA UDI

Identifiers

Catalog Number
05P8301 FDA UDI
Primary DI / UDI-DI
00380740100926 FDA UDI
FDA Product Code
JJX FDA UDI
JIT FDA UDI
GMDN Term
Lipoprotein A IVD, calibrator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
862.1150 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lipoprotein A IVD, calibrator

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

Similar devices

Also classified as Lipoprotein A IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a8ac5626-3db1-49b6-939b-0ab8deb82fbd 36 fields · synced May 30, 2026