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Atellica IM CEA MCM

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica IM CEA MCM FDA UDI
Generic Name
Carcinoembryonic antigen (CEA) IVD, control FDA UDI
Device Name
CEA - Atellica IM - Master Curve Material Kit 6 x 1 x 1.0mL FDA UDI
Model / Reference
10995526 FDA UDI
Description
CEA - Atellica IM - Master Curve Material Kit 6 x 1 x 1.0mL FDA UDI

Identifiers

Catalog Number
10995526 FDA UDI
Primary DI / UDI-DI
00630414598536 FDA UDI
510(k) Number
K981478 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Carcinoembryonic antigen (CEA) IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

Atellica IM CEA MCM by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a55f6a4c-35a2-40f1-81d3-72e54bdc563c 37 fields · synced Jun 6, 2026