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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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Armtragegurt — 11 UDI-DI variants, MDR (Tobler & Co. AG)

MD Atlas
Tobler & Co. AG

Data from EUDAMED, last updated May 23, 2026

Armtragegurt

764036657ATGSTRICKXG

11 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: Tobler & Co. AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764036657ATGSTRICKXG
Device name: —
Device model: Armtragegurt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: Tobler & Co. AG
SRN: CH-MF-000016205
Country: Switzerland
Email: info@tobler-coag.ch
Phone: +41 71 877 13 32

Authorised representative

Name: Tobler & Co. GmbH
SRN: LI-AR-000008357
Country: Liechtenstein

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01GVDNR81B7G3CDV989GZKH0D6

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

0351507640366570248
3351507640366571207
3351707640366571221
3352007640366571245
0351807640366570279
0351607640366570255
0351407640366570231
3351607640366571214
3351807640366571238
0351707640366570262
0352007640366570286