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

447.36407611819881426
447.354S07611819883680
447.377S07611819881686
04.114.00207611819393325
447.360S07611819881600
447.355S07611819829411
447.35507611819829398
447.375S07611819881679
447.35407611819883673
447.364S07611819881624
04.114.002S07611819415980
447.37707611819881488
447.37507611819881471
04.114.00407611819393349
447.36007611819881402
04.114.004S07611819416017
421.320S07611819270077
04.130.35507611819688858
04.130.36307611819688889
04.130.258S07612334091796
04.114.007S07611819416055
04.130.257S07612334091789
04.130.15307611819687691
04.130.159S07611819692060
04.130.25207611819688247

1 2 3 4 5