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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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Otalgan Cerunex — 2 UDI-DI variants, MDR (Verfora SA)

MD Atlas
Verfora SA

Data from EUDAMED, last updated May 23, 2026

Otalgan Cerunex

764024915OTCERFP

2 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: Verfora SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764024915OTCERFP
Device name: Otalgan Cerunex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: Verfora SA
SRN: CH-MF-000027018
Country: Switzerland
Email: info@verfora.ch
Phone: +41 58 851 93 00

Authorised representative

Name: Dr. A. & L. Schmidgall GmbH und Co. KG
SRN: AT-AR-000013703
Country: Austria
Phone: +438115814

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KAZT9J5V6E7MQCT5M9SQRP33

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

PF068507640102471495
PF068507640339781800