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

ET/05/08 — Class I MDR by FDI FRANCE

MD Atlas
FDI FRANCE

EUDAMED last updated this device on Jan 5, 2023

ET/05/08

3665155CanAngBT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FDI FRANCE
UDI-DI code: 03665155000847
Reference / catalog number: ET/05/08

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: FDI FRANCE
SRN: FR-MF-000023166
Manufacturer status: Active

Related devices

ASW/05/023665155CanAngBTOn the market ACO/01/023665155CanAngBTOn the market ACO/05/023665155CanAngBTOn the market ACO/04/023665155CanAngBTOn the market ACO/03/023665155CanAngBTOn 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

3 warnings recorded — scroll inside the panel to see all entries.

CW275
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW262
EUDAMED did not publish a description for this code.

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: not provided
UDI-DI code: 03665155000847
Basic UDI-DI: 3665155CanAngBT
Reference / catalog number: ET/05/08
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: ELBOW CRUTCH ERGOTECH WHITE GRIP : ORANGE
Additional information URL: https://www.fdifrance.com/
Clinical sizes: maxi 130 kgs

EMDN nomenclature code(s)

Y12030602CRUTCHES WITH ANTIBRACHIAL SUPPORT

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