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.

Aiming Device Coupling Screw… — 24 UDI-DI variants, MDR (Synthes GmbH)

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

Aiming Device Coupling Screw Screwdriver Push Block Holder Removal Tool Loading Station Torque Limiting Handle

7611819a00152J8

24 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: 7611819a00152J8
Device name: Aiming Device Coupling Screw Screwdriver Push Block Holder Removal Tool Loading Station Torque Limiting Handle
Device model: SYNFIX Evolution Instruments for Insertion and Extraction
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 14, 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

24 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

basicUdiUlid01K05822J6W20FDXW5Y7CXMA8A

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

03.835.00207611819658103
03.835.01507612334054364
03.835.00107611819658097
03.835.03607611819677098
03.835.10007611819682719
03.835.40207612334154675
03.835.01007611819658127
03.835.04307612334109460
03.835.04907611819682672
03.835.40307612334154682
03.835.07107611819682689
03.835.00607611819682665
03.835.40107612334154668
03.835.00407611819677043
03.835.41007612334154699
03.835.07007611819658240
03.835.03707612334005441
03.835.00307611819658110
03.835.41307612334154705
03.835.07207611819682696
03.835.00507611819677050
03.835.41607612334154712
03.835.03507611819677081
03.835.01307612334054357