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Elecsys Cortisol CalSet

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Elecsys Cortisol CalSet FDA UDI
Generic Name
Total cortisol IVD, calibrator FDA UDI
Model / Reference
11875124122 FDA UDI

Identifiers

Catalog Number
11875124122 FDA UDI
Primary DI / UDI-DI
04015630913084 FDA UDI
510(k) Number
K070788 FDA UDI
FDA Product Code
JIT FDA UDI
GMDN Term
Total cortisol IVD, calibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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

Yes

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, calibrator

Elecsys Cortisol CalSet by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total cortisol IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 40a34461-9b0a-445d-82b8-6ce0b507ce8d 35 fields · synced May 30, 2026