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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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TEDAVI — 10 UDI-DI variants, MDR (Schupp GmbH & Co. KG)

MD Atlas
Schupp GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

TEDAVI

4027887THERAPIELIEGEh77

10 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: Schupp GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4027887THERAPIELIEGEh77
Device name: TEDAVI
Device model: Therapy Table
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: Schupp GmbH & Co. KG
SRN: DE-MF-000010127
Country: Germany
Email: zentrale@schupp-gmbh.de
Phone: +49 7443 2430

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K1B5GC1PWJ6DH9YZQP3YFWVD

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

131035h04027887016067
138635h04027887016098
139435h04027887016005
136435h04027887016029
131435h04027887016081
14003504027887000042
140035h04027887016043
140235h04027887016050
140025h04027887016036
131235h04027887016074