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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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Retracting & repositioning instruments… — 1 UDI-DI variant, MDR

MD Atlas
Medartis AG

Data from EUDAMED, last updated May 23, 2026

Retracting & repositioning instruments (single use)

76300378013P9

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Medartis AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76300378013P9
Device name: Retracting & repositioning instruments (single use)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medartis AG
SRN: CH-MF-000022291
Country: Switzerland
Email: mario.dellacasa@medartis.com
Phone: +41 61 633 3565

Authorised representative

Name: Medartis GmbH
SRN: DE-AR-000005810
Country: Germany
Phone: +49 7665 98 24 0

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KP2YWXB4QAM108TTR1SCG2PV

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

Temporary Tension Bolt07630037896845