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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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Secutape Fixierung — 29 UDI-DI variants, MDR (Technimed AG)

MD Atlas
Technimed AG

Data from EUDAMED, last updated May 23, 2026

Secutape Fixierung

764015901secutape4T

29 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: Technimed AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764015901secutape4T
Device name: Secutape Fixierung
Device model: Secutape Grösse 2+
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Technimed AG
SRN: CH-MF-000028263
Country: Switzerland
Email: info@technimed.ch
Phone: +41 71 844 4920

Authorised representative

Name: SGT Servicegesellschaft Technipack mbH
SRN: DE-AR-000026432
Country: Germany
Phone: +49 8381 928380

Variants by status

UDI-DI variants

29 UDI-DI variants

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Applied filters

basicUdiUlid01KFBDCNBA4X010J1MV1DXASGC

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

850085007640159012405
850150007640159010531
850150907640159010555
850089007640159010432

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