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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

MD98000120 — Class I MDR by MEDIDEV - SENTECH FRANCE

MD Atlas
MEDIDEV - SENTECH FRANCE

EUDAMED last updated this device on Apr 27, 2026

MD98000120

376033037ADAPTATION1DD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDIDEV - SENTECH FRANCE
UDI-DI code: 03760330371085
Reference / catalog number: MD98000120

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Manufacturer information

Organization name: MEDIDEV - SENTECH FRANCE
SRN: FR-MF-000008021
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Jan 1, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760330371085
Basic UDI-DI: 376033037ADAPTATION1DD
Reference / catalog number: MD98000120
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: KIT ADAPTATION LARGEUR 120 cm POUR SENTRY 1200 ST : SUPPORT MOUSSE + HOUSSE
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12030102CONTINUOUS POSITIVE PRESSURE EQUIPMENT

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

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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.