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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

GYHBSV1Q8 — Class III MDD by Graftys

MD Atlas
Graftys

EUDAMED last updated this device on Jul 25, 2023

GYHBSV1Q8

B-03760177571235

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Graftys
UDI-DI code: 03760177571235
Reference / catalog number: GYHBSV1Q8

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Manufacturer information

Organization name: Graftys
SRN: FR-MF-000019838
Manufacturer status: Inactive

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW001
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW007
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	Dec 9, 2009	May 26, 2024

Device identification

Trade name: not provided
UDI-DI code: 03760177571235
Basic UDI-DI: B-03760177571235
Reference / catalog number: GYHBSV1Q8
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: GRAFTYS HBS - 8cc
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 8 MU12

EMDN nomenclature code(s)

P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES

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

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.

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