Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

BENTRIO — 2 UDI-DI variants, MDR (Altamira Medica AG)

MD Atlas
Altamira Medica AG

Data from EUDAMED, last updated May 23, 2026

BENTRIO

7649998266BNW3

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Altamira Medica AG

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Registered: No

Identity & classification

Basic UDI-DI: 7649998266BNW3
Device name: BENTRIO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Altamira Medica AG
SRN: CH-MF-000044549
Country: Switzerland
Email: QA@altamiramedica.com
Phone: +41 61 201 13 50

Authorised representative

Name: Johner Medical GmbH
SRN: DE-AR-000011832
Country: Germany

Variants by status

UDI-DI variants

2 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KAKDRRVE5R3VAR5780JVXVP1

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

BENTRIO07649998266208
BN-NOSEDK-0407649998266215