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Architect

FDA UDI

Class I (US FDA UDI)

by Abbott

Identity

Trade Name
ARCHITECT FDA UDI
Generic Name
Prealbumin (transthyretin) IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Prealbumin FDA UDI
Model / Reference
1E02-22 FDA UDI
Description
Prealbumin FDA UDI

Identifiers

Catalog Number
01E0222 FDA UDI
Primary DI / UDI-DI
00380740174897 FDA UDI
FDA Product Code
JZJ FDA UDI
GMDN Term
Prealbumin (transthyretin) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.5060 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: Prealbumin (transthyretin) IVD, kit, nephelometry/turbidimetry

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

Similar devices

Also classified as Prealbumin (transthyretin) IVD, kit, nephelometry/turbidimetry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott

Sources (1)

  • FDA UDI 22679f10-1708-48d6-b4d2-5d69d7a16ce2 36 fields · synced Jun 1, 2026