← Back to catalogue

IMMULITE® 2000 Systems COR Cortisol

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
IMMULITE® 2000 Systems COR Cortisol FDA UDI
Generic Name
Total cortisol IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
Cortisol - IMMULITE - RGT - 600 Tests FDA UDI
Model / Reference
10381480 FDA UDI
Description
Cortisol - IMMULITE - RGT - 600 Tests FDA UDI

Identifiers

Catalog Number
L2KCO6 FDA UDI
Primary DI / UDI-DI
00630414961194 FDA UDI
510(k) Number
K931409 FDA UDI
FDA Product Code
CGR 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

Yes

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

IMMULITE® 2000 Systems COR Cortisol by Siemens Healthcare Diagnostics Products Ltd — 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

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

Manufacturer

Sources (1)

  • FDA UDI 531b572c-06e6-41a5-8edd-1470cb559848 37 fields · synced May 30, 2026