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Atellica IM Cor

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica IM Cor FDA UDI
Generic Name
Total cortisol IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
Cortisol - Atellica IM - RGT 50T FDA UDI
Model / Reference
10995538 FDA UDI
Description
Cortisol - Atellica IM - RGT 50T FDA UDI

Identifiers

Catalog Number
10995538 FDA UDI
Primary DI / UDI-DI
00630414598659 FDA UDI
510(k) Number
K142723 FDA UDI
FDA Product Code
JFT FDA UDI
GMDN Term
Total cortisol IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1205 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: Total cortisol IVD, kit, chemiluminescent immunoassay

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

Similar devices

Also classified as Total cortisol IVD, kit, chemiluminescent immunoassay.

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 5e518339-0d67-4d37-815f-dcc452505548 37 fields · synced Jun 6, 2026