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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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Bowed Stem Extension Trial — 18 UDI-DI variants, MDR

MD Atlas
DePuy Ireland UC

Data from EUDAMED, last updated May 24, 2026

Bowed Stem Extension Trial

0603295a0019692

18 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: 0603295a0019692
Device name: Bowed Stem Extension Trial
Device model: LPS Bowed Stem Extension 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

18 UDI-DI variants

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Applied filters

basicUdiUlid01KDQSXZ7CYMFC2ZDQ9QP12RBC

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

LPS10603295157977
LPS10603295157915
LPS10603295158004
LPS10603295157885
LPS10603295158042
LPS10603295158059
LPS10603295157991
LPS10603295157939
LPS10603295158028
LPS10603295157922
LPS10603295157892
LPS10603295158035
LPS10603295157953
LPS10603295157908
LPS10603295157946
LPS10603295157984
LPS10603295157878
LPS10603295158011