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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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BIP Foley Catheter - Silicone — 55 UDI-DI variants, MDR

MD Atlas
Bactiguard AB

Data from EUDAMED, last updated May 30, 2026

BIP Foley Catheter - Silicone

7333330FOLEYSIL120101ZR

55 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: Bactiguard AB

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 2253382CE02
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: DEKRA Certification B.V. (0344)
Validity: Feb 9, 2024 → Jan 1, 2028

Identity & classification

Basic UDI-DI: 7333330FOLEYSIL120101ZR
Device name: BIP Foley Catheter - Silicone
Device model: BIP Foley Catheter - Silicone
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Bactiguard AB
SRN: SE-MF-000020790
Country: Sweden
Email: info@bactiguard.com
Phone: +46 8 440 58 80

Variants by status

UDI-DI variants

55 UDI-DI variants

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Applied filters

basicUdiUlid01JPHMZZF3XK2BHNHBBQ96GEX9

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.