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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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Double-ended dissector — 1 UDI-DI variant, MDR (Oticon Medical AB)

MD Atlas
Oticon Medical AB

Data from EUDAMED, last updated May 30, 2026

Double-ended dissector

5712149100178H

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Oticon Medical AB

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 5712149100178H
Device name: Double-ended dissector
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 31, 2023

Manufacturer & authorised representative

Manufacturer

Name: Oticon Medical AB
SRN: SE-MF-000000724
Country: Sweden
Email: kije@oticonmedical.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01G1K04EYN470P62306QYS2RK0

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

Double-ended dissector05712149008872