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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

PODOBAROSCOPE A ECLAIRAGE… — Class I MDR by CAPRON PODOLOGIE

MD Atlas
CAPRON PODOLOGIE

EUDAMED last updated this device on May 28, 2026

PODOBAROSCOPE A ECLAIRAGE TANGENTIEL A LED DE COULEURS - VERSION SCHEIN - SWISSBIOMECHANICS

37014885BA606827

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CAPRON PODOLOGIE
UDI-DI code: 03701488500019
Reference / catalog number: 6068-S-SBM

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View device family (Basic UDI)

Manufacturer information

Organization name: CAPRON PODOLOGIE
SRN: FR-MF-000000322
Manufacturer status: Active

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FEET PRINT - MACHINE DE THERMOFORMAGE AVEC CORRECTEUR DE VOUTE37014885BA794035On the market FEET PRINT EXPERT AVEC COUVERCLE DE PRESSAGE37014885BA794035On the market LAME DE GOUGE À USAGE UNIQUE STÉRILESB-37014885BA13002T8W5On the market MANCHE DE GOUGE INOX POUR LAMES DE GOUGES CAPRON37014885BA13000T4On the market MOBI - CONSOLE PEDICURIE 3 FOUETS - AVEC SERINGUE - BLANCHE37014885BA10790UDOn the market

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.

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
Germany		Still on market

Device identification

Trade name: PODOBAROSCOPE A ECLAIRAGE TANGENTIEL A LED DE COULEURS - VERSION SCHEIN - SWISSBIOMECHANICS
UDI-DI code: 03701488500019
Basic UDI-DI: 37014885BA606827
Reference / catalog number: 6068-S-SBM
Issuing entity: GS1

Classification

Risk category: Class I
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)03701488500019

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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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