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.

Passeo-35 Xeo — 162 UDI-DI variants, MDR (BIOTRONIK AG)

MD Atlas
BIOTRONIK AG

Data from EUDAMED, last updated May 31, 2026

Passeo-35 Xeo

76401304BUDI00017GL

162 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: BIOTRONIK 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

Identity & classification

Basic UDI-DI: 76401304BUDI00017GL
Device name: Passeo-35 Xeo
Device model: Passeo-35 Xeo 6/200/90
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: BIOTRONIK AG
SRN: CH-MF-000010176
Country: Switzerland
Email: VIInfo@teleflex.com
Phone: +41 (0) 44 864 5111

Authorised representative

Name: Teleflex Medical
SRN: IE-AR-000015869
Country: Ireland
Phone: 353 (0) 9 06 46 08 00

Variants by status

UDI-DI variants

162 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

basicUdiUlid01KSQEM0QZ3CMYFJK8DRV4QSZG

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

No registered UDI-DI variants for this device family.