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Architect

FDA UDI

Class II (US FDA UDI)

by Abbott

Identity

Trade Name
ARCHITECT FDA UDI
Generic Name
Total immunoglobulin A (IgA total) IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Immunoglobulin A FDA UDI
Model / Reference
9D98-22 FDA UDI
Description
Immunoglobulin A FDA UDI

Identifiers

Catalog Number
09D9822 FDA UDI
Primary DI / UDI-DI
00380740175177 FDA UDI
FDA Product Code
CZP FDA UDI
GMDN Term
Total immunoglobulin A (IgA total) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5510 FDA UDI
Commercial Distribution
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott

Sources (1)

  • FDA UDI b2b9d581-eb77-41b3-ac26-8aff589dffb2 37 fields · synced May 30, 2026