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

Paire de repose pied simple 16mm — Class I MDR by OBRO

MD Atlas
OBRO

EUDAMED last updated this device on May 30, 2024

Paire de repose pied simple 16mm

376039415020BU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: OBRO
UDI-DI code: 03760394150169
Reference / catalog number: CS316-16

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: OBRO
SRN: FR-MF-000019841
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: Paire de repose pied simple 16mm
UDI-DI code: 03760394150169
Basic UDI-DI: 376039415020BU
Reference / catalog number: CS316-16
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: Paire de repose pied à simple avec palette de pied. Réalisée en tubes carrés de 16 mm. Thermolaquage noir sablé pour l’ensemble des éléments.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12130280ORTHOPAEDIC TRACTION INSTRUMENTS – HARDWARE ACCESSORIES

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

Related devices

Mât pour sangle 25 mm376039415040C2On the market Articulation libre376039415040C2On the market Articulation libre déportée376039415040C2On the market Boîtier pour rallonge aluminium376039415040C2On the market Bouton étoile M8X15376039415040C2On 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.