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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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Scissors — 10 UDI-DI variants, MDR (Johnson & Johnson Medical GmbH)

MD Atlas
Johnson & Johnson Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Scissors

0705031a000063V

10 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: Johnson & Johnson Medical GmbH

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Device characteristics

Active deviceReusable

Identity & classification

Basic UDI-DI: 0705031a000063V
Device name: Scissors
Device model: Powerstar
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 14, 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

10 UDI-DI variants

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Applied filters

basicUdiUlid01KA1B0960WMKEF9MW5GFFHGY2

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

POWERSTAR10705031135161
POWERSTAR10705031135109
POWERSTAR10705031135130
POWERSTAR10705031135154
POWERSTAR10705031135093
POWERSTAR10705031135116
POWERSTAR10705031135079
POWERSTAR10705031135123
POWERSTAR10705031135147
POWERSTAR10705031135086