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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

Reamer with blade L 9mm diameter… — Class I MDD by movmedix

MD Atlas
movmedix

EUDAMED last updated this device on May 22, 2026

Reamer with blade L 9mm diameter 8mm

B-03700435646718

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: movmedix
UDI-DI code: 03700435646718
Reference / catalog number: D39012

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Manufacturer information

Organization name: movmedix
SRN: FR-MF-000000914
Manufacturer status: Active

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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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Jan 1, 2015	Still on market

Device identification

Trade name: Reamer with blade L 9mm diameter 8mm
UDI-DI code: 03700435646718
Basic UDI-DI: B-03700435646718
Reference / catalog number: D39012
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC 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: 9 MU50
8 MU50

EMDN nomenclature code(s)

L090999ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - 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