Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Femoral IM Connector — 16 UDI-DI variants, MDR (DePuy Ireland UC)

MD Atlas
DePuy Ireland UC

Data from EUDAMED, last updated May 24, 2026

Femoral IM Connector

0603295a001768U

16 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0603295a001768U
Device name: Femoral IM Connector
Device model: ATTUNE KNEE SYSTEM Femoral IM Connector
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

16 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KDQSXYQVY3JATR6V4SZGZS9S

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 SYSTEM10603295442738
ATTUNE KNEE SYSTEM10603295442844
ATTUNE KNEE SYSTEM10603295442783
ATTUNE KNEE SYSTEM10603295442837
ATTUNE KNEE SYSTEM10603295442790
ATTUNE KNEE SYSTEM10603295442820
ATTUNE KNEE SYSTEM10603295442752
ATTUNE KNEE SYSTEM10603295442769
ATTUNE KNEE SYSTEM10603295442806
ATTUNE KNEE SYSTEM10603295442745
ATTUNE KNEE SYSTEM10603295442851
ATTUNE KNEE SYSTEM10603295442813
ATTUNE KNEE SYSTEM10603295442776
ATTUNE KNEE SYSTEM10603295442868
ATTUNE KNEE SYSTEM10603295442714
ATTUNE KNEE SYSTEM10603295442721