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 - Stainless Steel — 126 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Hand Plates - Stainless Steel

7611819a00599KN

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: 7611819a00599KN
Device name: Hand Plates - Stainless Steel
Device model: LCP Compact Hand Plates, VA Locking Hand Plates, Adaption Plates, T-Adaption Plates, Y- Adaption Plates, Strut Plates - Stainless Steel
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

basicUdiUlid01K39QFTNNFY9B4JPMX9PQCHKS

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

02.130.263S07612334091659
02.130.36207611819688650
02.130.261S07612334091635
221.321S07611819921061
02.130.25607611819687929
02.130.366S07611819691759
221.312S07611819921047
02.114.01007611819392595
02.130.355S07611819691711
02.130.15107611819687479
02.130.158S07611819691636
02.130.264S07612334091666
02.130.15207611819687486
02.130.15007611819687462
221.334S07611819921085
221.32007611819100114
02.130.354S07611819691704
02.130.36607611819688674
02.130.161S07611819691650
02.130.253S07612334091550
02.130.25407611819687905
02.130.260S07612334091628
02.130.26007611819687967
221.33507611819100152
02.130.25307611819687899

2 3 4 5 6