Pricing Sign in

Role
Country
Date of registration
Address

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.

Organization name
UDI-DI code
Reference / catalog number

10000012 — Class IIa MDR by Biocool AB

MD Atlas
Biocool AB

EUDAMED last updated this device on Apr 22, 2026

10000012

739205910BPPFCCA

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Biocool AB
UDI-DI code: 07392059101764
Reference / catalog number: 10000012

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?

View device family (Basic UDI)

Manufacturer information

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

Related devices

BPPFC250EU739205910BPPFCCAOn the market BIOpH+ Footcare739205910BPPFCCAOn the market BPPFC500EU739205910BPPFCCAOn the market BIOpH+ Medical foot bath739205910BPPFCCAOn the market BIOpH+ Psoriasis medical bath739205910BPPPMBGGOn the market

Certificates

Certificate health across this manufacturer's portfolio.

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

Critical warnings

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

CW010
– Außerhalb der Reichweite von Kindern, beiRaumtemperatur und nicht zusammen mit oderin der Nähe von entzündlichen Produkten aufbewahren. – Die Anwendung bei schwangeren und stillenden Frauenwurde nicht getestet. Daher kann das Produkt für dieseGruppe nicht empfohlen werden. - Nicht auf offenen Wunden anwenden. Kontakt mit den Augen vermeiden, da dies zu Reizungen führen kann. Bei Augenkontakt mindestens 10 Minuten lang gründlich mit lauwarmem Wasser spülen. Nach Gebrauch die Hände gründlich waschen. Bei schweren Haut- oder Augenreizungen einen Arzt aufsuchen. - Bei unsachgemäßer Anwendung oder bei Überempﬁndlichkeit gegen Natriumpercarbonat kann es zu Hautreizungen kommen. - Nur zur äußerlichen Anwendung an den Füßen vorgesehen. - Kann nach der Behandlung zu rutschigen Füßen/Böden führen. Trocknen Sie Ihre Füße nach der Behandlung mit einem sauberen Handtuch ab. - Nicht verwenden, wenn die Dose beschädigt ist oder die Versiegelung an einer neuen Dose fehlt. Zum sicheren Öffnen des Deckels die Versiegelung in Pfeilrichtung abziehen.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Apr 17, 2026	Apr 17, 2099

Device identification

Trade name: not provided
UDI-DI code: 07392059101764
Basic UDI-DI: 739205910BPPFCCA
Reference / catalog number: 10000012
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: Medizinische Behandlung, diedie Symptome von Fußpilz (Hautrötung, Hautläsionen,Mazeration, Juckreiz, Kribbeln, Hyperkeratose undschlechter Geruch), rissige Fersen und Hornhaut reduziert, 250g.
Additional information URL: No additional information URL provided by the manufacturer.
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)07392059101764

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

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

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

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

Become a partner of MD Atlas