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.

Hand Plates - Titanium — 126 UDI-DI variants, MDR (Synthes GmbH)

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Hand Plates - Titanium

7611819a00600JE

126 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Synthes GmbH

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

Implantable

Identity & classification

Basic UDI-DI: 7611819a00600JE
Device name: Hand Plates - Titanium
Device model: LCP Compact Hand Plates, VA Locking Hand Plates, Adaption Plates, T-Adaption Plates, Y- Adaption Plates, Strut Plates - Titanium
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: Synthes GmbH
SRN: CH-MF-000013345
Country: Switzerland
Email: EUDAMED_Enquiries@its.jnj.com
Phone: +41 (0) 61 965 61 11

Authorised representative

Name: DePuy Ireland UC
SRN: IE-AR-000009328
Country: Ireland
Phone: +353 (0)21 4914000

Variants by status

UDI-DI variants

126 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

basicUdiUlid01K39QFR19KSCC5XSN0M9SZZ2G

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

04.130.354S07611819692121
04.130.36707611819688902
04.130.15407611819687707
04.130.25807611819688308
04.114.009S07611819416079
04.130.254S07612334091758
04.130.26207611819688346
04.130.25707611819688292
04.130.259S07612334091802
04.130.260S07612334091819
04.130.352S07611819692107
04.130.25107611819688230
421.32107611819084117
04.130.355S07611819692138
421.33407611819071087
04.130.36607611819688896
04.130.360S07611819692145
04.130.26707611819688377
04.114.00707611819393370
421.306S07611819270053
04.130.26807611819688384
421.33507611819071094
04.130.25907611819688315
04.130.35407611819688841
04.130.36207611819688872

2 3 4 5 6