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.

External orthopaedic fixation system… — 245 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

External orthopaedic fixation system component multiple use

7611819a00014HT

245 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7611819a00014HT
Device name: External orthopaedic fixation system component multiple use
Device model: External orthopaedic fixation system component multiple use
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 8, 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

245 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

basicUdiUlid01K4N64KPHD6GD8TNPARKQ19HN

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

03.311.31507611819872837
392.36007611819024908
393.97107611819041103
393.52007611819025325
03.311.11007611819872615
393.97007611819025578
03.311.81407611819873148
395.77907611819142763
03.311.05807611819411401
03.311.09007611819872561
393.51007611819025318
03.311.05107611819872462
394.970.1007611819322035
395.64007611819026223
03.311.81607611819873162
392.71007611819025059
03.311.31007611819872783
03.311.37807611819872974
03.311.20407611819872714
03.311.96407611819411524
03.311.13507611819872677
392.94307611819094093
395.67007611819026254
03.311.10807611819872608
392.94207611819093652

2 3 4 5 6