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.

Insert Trial — 432 UDI-DI variants, MDR (DePuy Ireland UC)

MD Atlas
DePuy Ireland UC

Data from EUDAMED, last updated May 24, 2026

Insert Trial

0603295a001588S

432 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: 0603295a001588S
Device name: Insert Trial
Device model: SIGMA Insert Trial
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 29, 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

432 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

basicUdiUlid01KDP3FVP5AG565Q6ZHJDT2V2M

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 SYSTEM10603295476825
ATTUNE KNEE SYSTEM10603295476856
ATTUNE KNEE SYSTEM10603295477167
ATTUNE KNEE SYSTEM10603295482017
ATTUNE KNEE SYSTEM10603295476245
ATTUNE KNEE SYSTEM10603295476160
ATTUNE KNEE SYSTEM10603295476269
ATTUNE KNEE SYSTEM10603295481935
ATTUNE KNEE SYSTEM10603295475958
ATTUNE KNEE SYSTEM10603295476009
ATTUNE KNEE SYSTEM10603295476788
ATTUNE KNEE SYSTEM10603295476252
ATTUNE KNEE SYSTEM10603295476917
ATTUNE KNEE SYSTEM10603295475842
ATTUNE KNEE SYSTEM10603295477228
ATTUNE KNEE SYSTEM10603295475903
ATTUNE KNEE SYSTEM10603295476726
ATTUNE KNEE SYSTEM10603295475309
ATTUNE KNEE SYSTEM10603295476276
ATTUNE KNEE SYSTEM10603295475415
ATTUNE KNEE SYSTEM10603295477532
ATTUNE KNEE SYSTEM10603295476894
ATTUNE KNEE SYSTEM10603295477211
ATTUNE KNEE SYSTEM10603295477433
ATTUNE KNEE SYSTEM10603295476719