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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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BIOpH+ Footcare — 5 UDI-DI variants, MDR (Biocool AB)

MD Atlas
Biocool AB

Data from EUDAMED, last updated May 30, 2026

BIOpH+ Footcare

739205910BPPFCCA

5 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: Biocool AB

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 28620160593
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: Intertek Medical Notified Body AB (2862)
Validity: Oct 26, 2023 → Oct 5, 2028

Identity & classification

Basic UDI-DI: 739205910BPPFCCA
Device name: BIOpH+ Footcare
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 24, 2024

Manufacturer & authorised representative

Manufacturer

Name: Biocool AB
SRN: SE-MF-000012411
Country: Sweden
Email: kontakt@biocool.se

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01HYNCCMB2Y0FJA3PW7TCYCDSJ

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

1000001207392059101764
BPPFC500EU07392059101580
BIOpH+ Footcare07392059101597
BPPFC250EU07392059101573
BIOpH+ Medical foot bath07392059101726