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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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LIGACLIP Applier — 12 UDI-DI variants, MDR

MD Atlas
Johnson & Johnson Medical GmbH

Data from EUDAMED, last updated May 23, 2026

LIGACLIP Applier

0705031a008034X

12 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: Johnson & Johnson Medical GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 0705031a008034X
Device name: LIGACLIP Applier
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Johnson & Johnson Medical GmbH
SRN: DE-MF-000007714
Country: Germany
Email: eudamed_enquiries@its.jnj.com

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K7SEVCYFFQD4EBR69HH1PRW2

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

LIGACLIP10705031135284
LIGACLIP10705031135383
LIGACLIP10705031135307
LIGACLIP10705031135345
LIGACLIP10705031135253
LIGACLIP10705031135352
LIGACLIP10705031135406
LIGACLIP10705031135314
LIGACLIP10705031135390
LIGACLIP10705031135369
LIGACLIP10705031135260
LIGACLIP10705031135291