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C-Stem

FDA UDI

Class II (US FDA UDI)

by Depuy International Ltd

Identity

Trade Name
C-STEM FDA UDI
Generic Name
Femoral stem centralizer FDA UDI
Device Name
C-STEM VOID CENTRALISER 18mm FDA UDI
Model / Reference
9612-18-500 FDA UDI
Description
C-STEM VOID CENTRALISER 18mm FDA UDI

Identifiers

Catalog Number
961218500 FDA UDI
Primary DI / UDI-DI
10603295235897 FDA UDI
510(k) Number
K013350 FDA UDI
K982918 FDA UDI
FDA Product Code
JDI FDA UDI
GMDN Term
Femoral stem centralizer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Femoral stem centralizer

C-Stem by Depuy International Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femoral stem centralizer.

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 e70990ca-181e-457f-8d6a-5f48f5163b02 36 fields · synced Jun 6, 2026