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.

LCP Superior Anterior 2.7/3.5 , LCP… — 66 UDI-DI variants, MDR

MD Atlas
Synthes GmbH

Data from EUDAMED, last updated May 23, 2026

LCP Superior Anterior 2.7/3.5 , LCP Superior 2.7/3.5 and LCP Anterior 3.5 Clavicle Plate TAN

7611819a00670K3

66 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: 7611819a00670K3
Device name: LCP Superior Anterior 2.7/3.5 , LCP Superior 2.7/3.5 and LCP Anterior 3.5 Clavicle Plate TAN
Device model: LCP Superior Anterior 2.7/3.5 , LCP Superior 2.7/3.5 and LCP Anterior 3.5 Clavicle Plate TAN
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

66 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

basicUdiUlid01K1EEHJY260W7YT4YZPVJ4X9D

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

04.112.027S07611819310025
04.112.091S07611819437234
04.112.090S07611819437227
04.112.007S07611819309944
04.112.013S07611819360006
04.112.093S07611819437258
04.112.01207611819360075
04.112.02007611819309708
04.112.02707611819309739
04.112.01807611819309685
04.112.029S07611819310049
04.112.01307611819360082
04.112.028S07611819310032
04.112.09407611819437029
04.112.09107611819436992
04.112.08507611819436978

1 2 3