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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Shim C-I — 10 UDI-DI variants, MDR (DePuy Ireland UC)

MD Atlas
DePuy Ireland UC

Data from EUDAMED, last updated May 24, 2026

Shim C-I

0603295a000448A

10 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: DePuy Ireland UC

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0603295a000448A
Device name: Shim C-I
Device model: ATTUNE KNEE SYSTEM Shim C-I
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: DePuy Ireland UC
SRN: IE-MF-000007377
Country: Ireland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +353 (0)214914000

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KRH8TZSVBVG2FSJVPYT54HNP

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

ATTUNE KNEE SYSTEM10603295490395
ATTUNE KNEE SYSTEM10603295490340
ATTUNE KNEE SYSTEM10603295490333
ATTUNE KNEE SYSTEM10603295490388
ATTUNE KNEE SYSTEM10603295490364
ATTUNE KNEE SYSTEM10603295490371
ATTUNE KNEE SYSTEM10603295490357
ATTUNE KNEE SYSTEM10603295490401
ATTUNE KNEE SYSTEM10603295490425
ATTUNE KNEE SYSTEM10603295490418