Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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

Gouge Pédicure tranchante 18mm — Class I MDD

MD Atlas
Ets Claude LASSERTEUX S.A

EUDAMED last updated this device on Feb 24, 2026

Gouge Pédicure tranchante 18mm

B-03701675301979

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Ets Claude LASSERTEUX S.A
UDI-DI code: 03701675301979
Reference / catalog number: 880031.18

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?

Manufacturer information

Organization name: Ets Claude LASSERTEUX S.A
SRN: FR-MF-000001821
Manufacturer status: Active

Related devices

Abaisse-langue Chatellier 20mmB-03701675327795On the market Abaisse-langue Chatellier 25mmB-03701675327788On the market Abaisse-langue Chatellier 30mmB-03701675327771On the market Abaisse-langue Lecouteur 27 x 23mmB-03701675327801On the market Abaisse-langue Saint Germain 17mmB-03701675327764On the market

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: Gouge Pédicure tranchante 18mm
UDI-DI code: 03701675301979
Basic UDI-DI: B-03701675301979
Reference / catalog number: 880031.18
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC 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.

EMDN nomenclature code(s)

L2499DERMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.