← Back to catalogue

Alinity

FDA UDI

Class II (US FDA UDI)

by Abbott Ireland Diagnostics

Identity

Trade Name
Alinity FDA UDI
Generic Name
Carcinoembryonic antigen (CEA) IVD, control FDA UDI
Device Name
Alinity i CEA Controls FDA UDI
Model / Reference
07P6210 FDA UDI
Description
Alinity i CEA Controls FDA UDI

Identifiers

Catalog Number
07P6210 FDA UDI
Primary DI / UDI-DI
00380740130848 FDA UDI
FDA Product Code
DHX FDA UDI
GMDN Term
Carcinoembryonic antigen (CEA) IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.6010 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: Carcinoembryonic antigen (CEA) IVD, control

Alinity by Abbott Ireland Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carcinoembryonic antigen (CEA) IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 08db0637-9027-4ebb-9ec7-9c860397925b 36 fields · synced Jun 1, 2026