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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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THERY UAG — 3 UDI-DI variants, MDR (TEDIRO Healthcare Robotics GmbH)

MD Atlas
TEDIRO Healthcare Robotics GmbH

Data from EUDAMED, last updated May 23, 2026

THERY UAG

426248145THERYUAG84

3 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: TEDIRO Healthcare Robotics GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426248145THERYUAG84
Device name: THERY UAG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: TEDIRO Healthcare Robotics GmbH
SRN: DE-MF-000043787
Country: Germany
Email: service@tediro.com
Phone: +49 341 566 393 00

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JEV034ZF6YAS4KC770GK4NJC

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

TI_FA00000_0004262481450019
UAG04262481450026
TMS04262481450033