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Elecsys CPeptide CalSet

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Elecsys CPeptide CalSet FDA UDI
Generic Name
C-peptide IVD, calibrator FDA UDI
Model / Reference
3184919190 FDA UDI

Identifiers

Catalog Number
3184919190 FDA UDI
Primary DI / UDI-DI
04015630920112 FDA UDI
510(k) Number
K033873 FDA UDI
FDA Product Code
JIX FDA UDI
GMDN Term
C-peptide 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: C-peptide IVD, calibrator

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

Similar devices

Also classified as C-peptide IVD, calibrator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4b3bc9e7-9bb5-4cde-982c-51b1a77ada52 35 fields · synced May 29, 2026