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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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Organization name
UDI-DI code
Reference / catalog number

BIOpH+ Footcare — Class IIa MDR by Biocool AB

MD Atlas
Biocool AB

EUDAMED last updated this device on Apr 22, 2026

BIOpH+ Footcare

739205910BPPFCCA

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Biocool AB
UDI-DI code: 07392059101597
Reference / catalog number: BPPFC1250EU

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View device family (Basic UDI)

Manufacturer information

Organization name: Biocool AB
SRN: SE-MF-000012411
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
- Skall förvaras oåtkomligt för barn, i rumstemperatur och ej tillsammans eller i närheten av brandfarliga produkter. - Användning av gravida och ammande kvinnor har ej testats. Därav kan produkten ej rekommenderas för denna grupp. - Skall ej användas på öppna sår, undvik kontakt med ögon, kan orsaka irritation. Om produkten kommer i kontakt med ögon, skölj noggrant med ljummet vatten i minst tio minuter. Tvätta händerna grundligt efter användning. Kontakta sjukvård om allvarlig hud- eller ögonirritation uppkommer. - Om produkten används på fel sätt eller om överkänslighet mot natriumperkarbonat föreligger kan detta orsaka hudirritation. - Endast avsedd för utvärtes bruk på fötter. - Kan orsaka hala fötter/golv. Torka fötterna med ren handduk efter behandling. - Använd ej om burken är skadad eller om plomberingen saknas på en ny burk. För säker öppning av locket, dra av plomberingen i pilens riktning.

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Market distribution

Primary placement in Sweden; available across 1 country total.

Country	On market since	Until
SwedenPrimary placement	Jan 7, 2026	May 1, 2090

Device identification

Trade name: BIOpH+ Footcare
UDI-DI code: 07392059101597
Basic UDI-DI: 739205910BPPFCCA
Reference / catalog number: BPPFC1250EU
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Medicinteknisk behandling som reducerar symtomen vid fotsvamp (hudrodnad, huderosioner, maceration, klåda, stickande känsla, hyperkeratos och odör), hälsprickor och förhårdnader..  1250 g
Additional information URL: https://biophplus.com/products/bioph-footcare
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07392059101597

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Certificates

Certificate health across this manufacturer's portfolio.

28620160593Issued
Quality management systemNotified body: 2862Expiry: Oct 5, 2028