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.

Orthopaedic Insertion and Extraction… — 128 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Orthopaedic Insertion and Extraction Instruments

7611819a00219JF

128 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

Reusable

Identity & classification

Basic UDI-DI: 7611819a00219JF
Device name: Orthopaedic Insertion and Extraction Instruments
Device model: Orthopaedic Insertion and Extraction Instruments
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
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

128 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

basicUdiUlid01K1EDZN7JBBWN2R5PB26BK1VM

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

03.010.42407611819376168
03.010.41407611819350915
03.010.41107611819349483
309.55207611819148666
309.55107611819148673
03.010.13107611819792050
359.21907611819096653
359.22007611819404403
359.20607611819096615
359.20507611819093034
03.037.02407611819642508
03.037.02507611819642515
03.037.02607611819642522
03.037.03007611819642560
357.54007611819056763
356.72207611819281233
357.36107611819071575
357.34007611819048416
357.36007611819048423
358.69707611819714830
358.69607611819714823
03.221.25007612334219251
03.045.00207612334167798
357.42807611819456945
356.33107611819074453

1 2 3 4 5