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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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Passeo-18 — 128 UDI-DI variants, MDR (BIOTRONIK AG)

MD Atlas
BIOTRONIK AG

Data from EUDAMED, last updated May 31, 2026

Passeo-18

76401304BUDI00003G9

128 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

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UDI-DI variants

128 UDI-DI variants

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Applied filters

basicUdiUlid01KSQEFVMKV2DTTJBFA22XA4R1

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

Passeo-1807640130414525
Passeo-1807640119558844
Passeo-1807640130414426
Passeo-1807640130430013
Passeo-1807640130414440
Passeo-1807640130414792
Passeo-1807640130414624
Passeo-1807640119558837
Passeo-1807640130414716
Passeo-1807640119558622
Passeo-1807640119559001
Passeo-1807640119559056
Passeo-1807640130414723
Passeo-1807640130414648
Passeo-1807640130414655
Passeo-1807640130430037
Passeo-1807640130430006
Passeo-1807640130429802
Passeo-1807640130429796
Passeo-1807640119558639
Passeo-1807640130429833
Passeo-1807640119558776
Passeo-1807640119558875
Passeo-1807640119559131
Passeo-1807640130429819

1 2 3 4 5

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76401304BUDI00003G9
Device name: Passeo-18
Device model: Passeo-18 7/200/130
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