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Atellica IM CpS

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica IM CpS FDA UDI
Generic Name
C-peptide IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
C-Peptide (CpS) Atellica IM - RGT 100T FDA UDI
Model / Reference
10995541 FDA UDI
Description
C-Peptide (CpS) Atellica IM - RGT 100T FDA UDI

Identifiers

Catalog Number
10995541 FDA UDI
Primary DI / UDI-DI
00630414600413 FDA UDI
FDA Product Code
JKD FDA UDI
GMDN Term
C-peptide IVD, kit, chemiluminescent immunoassay 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

No

FDA UDI

Category: C-peptide IVD, kit, chemiluminescent immunoassay

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

Similar devices

Also classified as C-peptide IVD, kit, chemiluminescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b3676814-ba96-43b8-a82a-44064d39c9ba 36 fields · synced May 30, 2026