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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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Ambu® Subdermal Corkscrew — 1 UDI-DI variant, MDD (Technomed Europe)

MD Atlas
Technomed Europe

Data from EUDAMED, last updated May 30, 2026

Ambu® Subdermal Corkscrew

B-08720791370862

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Technomed Europe

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 2109122CE01
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: DEKRA Certification B.V. (0344)
Validity: Oct 31, 2023

Identity & classification

Basic UDI-DI: B-08720791370862
Device name: Ambu® Subdermal Corkscrew
Device model: 74720-60/24
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Sep 29, 2023

Manufacturer & authorised representative

Manufacturer

Name: Technomed Europe
SRN: NL-MF-000000064
Country: Netherlands
Email: infotechnomed@welcony.com
Phone: +31 43 408 68 68

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01HBGAKBH5XFJMA369N121ZTWT

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

Ambu® Subdermal Corkscrew08720791370862