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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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LA/MI-Schlitzt.140x105-50 — 4 UDI-DI variants, MDR

MD Atlas
Rosa Toifl & Co GmbH

Data from EUDAMED, last updated May 23, 2026

LA/MI-Schlitzt.140x105-50

9010845OP-Tuch-BT

4 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: Rosa Toifl & Co GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 9010845OP-Tuch-BT
Device name: LA/MI-Schlitzt.140x105-50
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 23, 2023

Manufacturer & authorised representative

Manufacturer

Name: Rosa Toifl & Co GmbH
SRN: AT-MF-000020516
Country: Austria
Email: jtr@jtr.at
Phone: +43149315980

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GSZ8CDXBDMAP3METWQVY36SN

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

2310309010845011780
2310409010845011636
2310109010845010011
2310009010845010004