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

02.130.351S07611819691674
02.114.00307611819392533
02.114.003S07611819410572
02.130.25907611819687950
02.130.257S07612334091598
02.130.25007611819687868
02.130.255S07612334091574
02.130.262S07612334091642
02.130.15907611819687547
02.130.26507612334094810
221.320S07611819921054
02.130.25107611819687875
02.130.151S07611819690479
02.130.157S07611819691629
02.130.25807611819687943
02.130.36707611819688681
02.130.258S07612334091604
02.130.35507611819688636
02.130.15707611819687523
02.130.25207611819687882
02.130.152S07611819690486
02.130.36307611819688667
02.130.26807611819688025
02.114.01307611819392908
02.130.150S07611819690462

1 2 3 4 5