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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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LAME DE GOUGE À USAGE UNIQUE STÉRILES — 1 UDI-DI variant, MDD

MD Atlas
CAPRON PODOLOGIE

Data from EUDAMED, last updated May 19, 2026

LAME DE GOUGE À USAGE UNIQUE STÉRILES

B-37014885BA13002T8W5

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: CAPRON PODOLOGIE

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 10207
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: GMED SAS (0459)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-37014885BA13002T8W5
Device name: LAME DE GOUGE À USAGE UNIQUE STÉRILES
Device model: Réf : 13002-001 n°1, n°2, n°3, n°5, n°8, n°10, n°12
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 11, 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

1 UDI-DI variant

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Applied filters

basicUdiUlid01KRB5HB2CY07JBS1T5FDQE1ER

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

LAME DE GOUGE À USAGE UNIQUE STÉRILESD-37014885BA13002T8W5