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

FAUTEUIL QUADRICEPS STANDARD — Class I MDR by FIRN SARL

MD Atlas
FIRN SARL

EUDAMED last updated this device on Nov 4, 2025

FAUTEUIL QUADRICEPS STANDARD

376036522FAUTEUILSHE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FIRN SARL
UDI-DI code: 03760365220099
Reference / catalog number: 241050

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: FIRN SARL
SRN: FR-MF-000015675
Manufacturer status: Active

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: FAUTEUIL QUADRICEPS STANDARD
UDI-DI code: 03760365220099
Basic UDI-DI: 376036522FAUTEUILSHE
Reference / catalog number: 241050
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: FAUTEUIL QUADRICEPS ISCHIOS STANDARD
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12069099VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - 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.

Related devices

AVANCEE ESPALIER METAL376036522CAGES5LOn the market AXESS DUO D1376036522TABLESB7On the market AXESS DUO D2376036522TABLESB7On the market AXESS TRIO T1376036522TABLESB7On the market AXESS TRIO T3376036522TABLESB7On the market