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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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TeleScan — 7 UDI-DI variants, MDR (tomedo Praxissoftware Medizin GmbH)

MD Atlas
tomedo Praxissoftware Medizin GmbH

Data from EUDAMED, last updated May 23, 2026

TeleScan

42519867-TeleScan-B9

7 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: tomedo Praxissoftware Medizin GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42519867-TeleScan-B9
Device name: TeleScan
Device model: TeleScan
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Jan 24, 2023

Manufacturer & authorised representative

Manufacturer

Name: tomedo Praxissoftware Medizin GmbH
SRN: DE-MF-000028502
Country: Germany
Email: prrc@tpm.health
Phone: +49 3641 7979361

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GCZXAR06ZGADBEZS6ZXXPJ2Y

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

TS-APP-001-I04251986700002
TS-FA-001-W04251986700064
TS-FA-001-L04251986700057
TS-FA-001-M04251986700040
TS-HA-001-W04251986700033
TS-HA-001-M04251986700019
TS-HA-001-L04251986700026