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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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Organization name
UDI-DI code
Reference / catalog number

Michelin AirProne Tibias Module — Class I MDR

MD Atlas
Manufacture Française des Pneumatiques MICHELIN

EUDAMED last updated this device on Feb 28, 2023

Michelin AirProne Tibias Module

0086699AIRCV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Manufacture Française des Pneumatiques MICHELIN
UDI-DI code: 00086699900012
Reference / catalog number: 069545

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Manufacturer information

Organization name: Manufacture Française des Pneumatiques MICHELIN
SRN: FR-MF-000002723
Manufacturer status: Active

Related devices

Michelin AirProne Arm Module0086699AIRCVOn the market Michelin AirProne front Head Module0086699AIRCVOn the market Michelin AirProne Pelvis Module0086699AIRCVOn the market MICHELIN AirProne set0086699AIRCVOn the market Michelin AirProne Side Head Module0086699AIRCVOn 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.

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: Michelin AirProne Tibias Module
UDI-DI code: 00086699900012
Basic UDI-DI: 0086699AIRCV
Reference / catalog number: 069545
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12011299PATIENT POSITIONING 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

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Expiration date
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