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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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Instrument Case/Tray — 112 UDI-DI variants, MDR (DePuy Ireland UC)

MD Atlas
DePuy Ireland UC

Data from EUDAMED, last updated May 24, 2026

Instrument Case/Tray

0603295a000107R

112 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: 0603295a000107R
Device name: Instrument Case/Tray
Device model: TruMatch Instrument Case/Tray
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

112 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRH8BBTGHT7B1SG1T570KH3Q

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

9505-02-83310603295229599
9505-02-84710603295229728
9505-02-83410603295229605
9505-02-84110603295229667
9505-02-80810603295229360
9505-02-80410603295229322
9505-02-80310603295229315
9505-02-83010603295229568
9505-02-82610603295229537
9505-02-81310603295229414
9505-02-80710603295229353
9505-02-83610603295229629

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