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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

SDGM-ABCDHIJKLMPQR — Class IIb MDD by GAZ PURS ET FLUIDES

MD Atlas
GAZ PURS ET FLUIDES

EUDAMED last updated this device on Jan 24, 2022

SDGM-ABCDHIJKLMPQR

B-03770022435292

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: GAZ PURS ET FLUIDES
UDI-DI code: 03770022435292
Reference / catalog number: SDGM-ABCDHIJKLMPQR

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Manufacturer information

Organization name: GAZ PURS ET FLUIDES
SRN: FR-MF-000003878
Manufacturer status: Active

Critical warnings

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

CW133
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	Aug 8, 1998	May 26, 2024

Device identification

Trade name: not provided
UDI-DI code: 03770022435292
Basic UDI-DI: B-03770022435292
Reference / catalog number: SDGM-ABCDHIJKLMPQR
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: SDGM pour CENTRALE AIR BOUTEILLES - COMPRESSEUR D'AIR - GROUPE DE VIDE - BOUTEILLES N20 - GENERATEUR DE VIDE POUR GAZ ANESTHESIANTS - CHAMBRES HOSPITALISATION - REA - USIC - SOINS INTENSIFS - SALLE DE REVEIL SSPI - SALLE D'OPERATION - IMAGERIE AMBULATOIRE CONSULTATIONS DIALYSE CHIMIO - URGENCES - STERILISATION- LAVAGE- ENDOSCOPIE - PHARMACIE -ARMOIRE ULTIME SECOURS
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A99DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - 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

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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.