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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

GSIL — Class I MDR by Laboratoire Abiocom

MD Atlas
Laboratoire Abiocom

EUDAMED last updated this device on Mar 26, 2026

GSIL

3760177RollonTM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratoire Abiocom
UDI-DI code: 03760177500037
Reference / catalog number: GSIL51DM

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Manufacturer information

Organization name: Laboratoire Abiocom
SRN: FR-MF-000046820
Manufacturer status: Active

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: GSIL
UDI-DI code: 03760177500037
Basic UDI-DI: 3760177RollonTM
Reference / catalog number: GSIL51DM
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)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

Related devices

GSIL3760177RollonTMOn the market GSIL043760177RollonTMOn the market GSIL3760177RollonTMOn the market SILAGIC3760177RollonTMOn the market SILAGIC3760177RollonTMOn 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.