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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

Chasse Greffon cylindrique double… — Class I MDD

MD Atlas
Ets Claude LASSERTEUX S.A

EUDAMED last updated this device on Mar 3, 2026

Chasse Greffon cylindrique double 16cm 10 x 12mm

B-03701675305182

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Ets Claude LASSERTEUX S.A
UDI-DI code: 03701675305182
Reference / catalog number: 842030.12

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Manufacturer information

Organization name: Ets Claude LASSERTEUX S.A
SRN: FR-MF-000001821
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.

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: Chasse Greffon cylindrique double 16cm 10 x 12mm
UDI-DI code: 03701675305182
Basic UDI-DI: B-03701675305182
Reference / catalog number: 842030.12
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: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L0999ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY 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
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Software identification