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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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PODOGRAPH' — 6 UDI-DI variants, MDR (CAPRON PODOLOGIE)

MD Atlas
CAPRON PODOLOGIE

Data from EUDAMED, last updated May 30, 2026

PODOGRAPH'

37014885BA6055ZT

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: CAPRON PODOLOGIE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37014885BA6055ZT
Device name: PODOGRAPH'
Device model: PODOGRAPH'
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: CAPRON PODOLOGIE
SRN: FR-MF-000000322
Country: France
Email: contact@capronpodologie.com
Phone: +33 385779060

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KSHMSF7VGB91T8MJYQ1DRNY8

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

PODOGRAPH 1 PIED NU SANS FEUILLE D'EMPREINTES03701488505045
PODOGRAPH 2 PIEDS NU SANS FEUILLE D'EMPREINTES03701488505038
PODOGRAPH' 1 PIED - 25 FEUILLES D'EMPREINTES - ROULEAU ENCREUR - FLACON D'ENCRE03701488501771
PODOGRAPH'1 PIED - 25 FEUILLES D'EMPREINTES03701488505076
PODOGRAPH'2 PIEDS - 25 FEUILLES D'EMPREINTES03701488505052
PODOGRAPH'2 PIEDS - 25 FEUILLES D'EMPREINTES - ROULEAU ENCREUR - FLACON D'ENCRE03701488505069