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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

Dr. Scholl's Freeze Away MAX… — Class IIa MDR

MD Atlas
Pronova Laboratories BV

EUDAMED last updated this device on Mar 24, 2026

Dr. Scholl's Freeze Away MAX Traitement Verrues Cryothérapie

871734439FW10XXJ9

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Pronova Laboratories BV
UDI-DI code: 08717344390613
Reference / catalog number: FW10FRM100

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View device family (Basic UDI)

Manufacturer information

Organization name: Pronova Laboratories BV
SRN: NL-MF-000001486
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: Dr. Scholl's Freeze Away MAX Traitement Verrues Cryothérapie
UDI-DI code: 08717344390613
Basic UDI-DI: 871734439FW10XXJ9
Reference / catalog number: FW10FRM100
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: —
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)08717344390613

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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.

V0999FLUIDS/GASES FOR CLINICAL/THERAPEUTICAL USE - 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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Related devices

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.