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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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Endoscopic Forceps — 2 UDI-DI variants, MDR

MD Atlas
Johnson & Johnson Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Endoscopic Forceps

0705031a0080757

2 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: 0705031a0080757
Device name: Endoscopic Forceps
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 1, 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

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K6EF4SNHB35RY68RB90JB99C

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

ETHICON10705031135420
ETHICON10705031135413