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 Two-Column Volar Distal Radius… — 48 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

VA LCP Two-Column Volar Distal Radius Plate 2.4mm TiCP

7611819a00382JT

48 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: 7611819a00382JT
Device name: VA LCP Two-Column Volar Distal Radius Plate 2.4mm TiCP
Device model: VA LCP Two-Column Volar Distal Radius Plate 2.4mm TiCP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jul 30, 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

48 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

basicUdiUlid01K1EEHYJMXPYN9GS5S5AB757W

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

04.111.620S07611819354357
04.111.631S07611819354388
04.111.730S07611819354470
04.111.65007611819352643
04.111.53107611819391413
04.111.530S07611819392243
04.111.741S07611819354500
04.111.62107611819352599
04.111.64007611819352629
04.111.54107611819391437
04.111.630S07611819354371
04.111.63107611819352612
04.111.750S07611819354517
04.111.52007611819391383
04.111.55007611819391444
04.111.52107611819391390
04.111.72007611819352681
04.111.551S07611819392298
04.111.720S07611819354456
04.111.520S07611819392229
04.111.650S07611819354418
04.111.54007611819391420
04.111.75107611819352759
04.111.641S07611819354401
04.111.64107611819352636

1 2