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.

VA-LCP Distal Humerus Plate TAN — 100 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

VA-LCP Distal Humerus Plate TAN

7611819a00656K9

100 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: 7611819a00656K9
Device name: VA-LCP Distal Humerus Plate TAN
Device model: VA-LCP Distal Humerus Plate TAN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 11, 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

100 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

basicUdiUlid01JZXAAMB6V4YR7DAEV6A2EXKV

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

04.117.402S07611819504929
04.117.502S07611819504981
04.117.20707611819585768
04.117.907S07611819506251
04.117.805S07611819506183
04.117.213S07611819585997
04.117.708S07611819505735
04.117.410S07611819504967
04.117.50607611819505247
04.117.909S07611819506268
04.117.80707611819505957
04.117.011S07611819586390
04.117.10307611819506954
04.117.404S07611819504936
04.117.003S07611819505407
04.117.303S07611819506718
04.117.50107611819505216
04.117.00907611819586185
04.117.70407611819512467
04.117.207S07611819585966
04.117.702S07611819505704
04.117.506S07611819505001
04.117.60207611819512399
04.117.510S07611819505025
04.117.70107611819512443

1 2 3 4