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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

Anuscope moyen à bord droit sans… — Class I MDR

MD Atlas
Etablissements Albert Legrand

EUDAMED last updated this device on Jul 9, 2025

Anuscope moyen à bord droit sans poignée à usage unique

3701603412034QP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Etablissements Albert Legrand
UDI-DI code: 03701603400200
Reference / catalog number: 12.034/1

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Manufacturer information

Organization name: Etablissements Albert Legrand
SRN: FR-MF-000029888
Manufacturer status: Active

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: Anuscope moyen à bord droit sans poignée à usage unique
UDI-DI code: 03701603400200
Basic UDI-DI: 3701603412034QP
Reference / catalog number: 12.034/1
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: Single-use medium straight-ended proctoscope without grab handle
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

G02060301ANOSCOPES

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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