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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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Cathejell Mono — 3 UDI-DI variants, MDR

MD Atlas
Pharmazeutische Fabrik Montavit Ges.m.b.H.

Data from EUDAMED, last updated May 23, 2026

Cathejell Mono

9001505CATHEJELL004HF

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Pharmazeutische Fabrik Montavit Ges.m.b.H.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 9001505CATHEJELL004HF
Device name: Cathejell Mono
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Pharmazeutische Fabrik Montavit Ges.m.b.H.
SRN: AT-MF-000001620
Country: Austria
Email: pharma@montavit.com
Phone: 0043 5223 57926

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KQ9W1GSQS3XGAP2AE9R9A00T

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

40082609001505008264
40082509001505008257
40082409001505008240