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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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Isolation Transformer — 2 UDI-DI variants, MDR (Sentec AG)

MD Atlas
Sentec AG

Data from EUDAMED, last updated May 23, 2026

Isolation Transformer

764012188RFTKR

2 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: Sentec AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 764012188RFTKR
Device name: Isolation Transformer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 22, 2021

Manufacturer & authorised representative

Manufacturer

Name: Sentec AG
SRN: CH-MF-000008058
Country: Switzerland
Email: info@sentec.com

Authorised representative

Name: Sentec GmbH
SRN: DE-AR-000007618
Country: Germany

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FN3F950ER5RN4GZS3QK1QY7F

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

Isolation Transformer07640121880902
Isolation Transformer07640121880896