← Back to catalogue

Atellica IM CpS MCM

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica IM CpS MCM FDA UDI
Generic Name
C-peptide IVD, control FDA UDI
Device Name
C-Peptide (CpS) Atellica IM - Master Curve Material Kit 10 x 1 x 1.0mL FDA UDI
Model / Reference
10995543 FDA UDI
Description
C-Peptide (CpS) Atellica IM - Master Curve Material Kit 10 x 1 x 1.0mL FDA UDI

Identifiers

Catalog Number
10995543 FDA UDI
Primary DI / UDI-DI
00630414600437 FDA UDI
FDA Product Code
JKD FDA UDI
GMDN Term
C-peptide IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1135 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: C-peptide IVD, control

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

Similar devices

Also classified as C-peptide 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 9f005483-b9ce-422b-b3c0-f3aa5548208b 36 fields · synced Jun 6, 2026