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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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Base Trial — 11 UDI-DI variants, MDR (DePuy Ireland UC)

MD Atlas
DePuy Ireland UC

Data from EUDAMED, last updated May 24, 2026

Base Trial

0603295a0017992

11 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0603295a0017992
Device name: Base Trial
Device model: ATTUNE KNEE SYSTEM Base Trial
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 30, 2025

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

11 UDI-DI variants

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Applied filters

basicUdiUlid01KDQSRQ2X7AKDW2TSN279W2TP

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 SYSTEM10603295435907
ATTUNE KNEE SYSTEM10603295435853
ATTUNE KNEE SYSTEM10603295435884
ATTUNE KNEE SYSTEM10603295435822
ATTUNE KNEE SYSTEM10603295435877
ATTUNE KNEE SYSTEM10603295435846
ATTUNE KNEE SYSTEM10603295504955
ATTUNE KNEE SYSTEM10603295435914
ATTUNE KNEE SYSTEM10603295435860
ATTUNE KNEE SYSTEM10603295435891
ATTUNE KNEE SYSTEM10603295435921