Isolation Device Server Type II

Nom de l'organisation

Trium Analysis Online GmbH

SRN

DE-MF-000007016

Statut du fabricant

Actif

10 avertissements enregistrés — faire défiler le panneau pour tout voir.

• CW999

  Do not connect the IDS2 to a telephone outlet. Use this device only attached to an Ethernet computer network.
• CW999

  Do not modify this equipment without authorization of the manufacturer.
• CW999

  Accessory equipment or cables not in accordance with this instructions may cause either harmful electromagnetic interference or result in a reduced protection of the device. It is possible that radio-frequency transmitting equipment in close proximity may result in disruption of performance of this device. The operator is encouraged to determine the electromagnetic compatibility before this equipment is used for the first time.
• CW999

  The IDS2 should not be used adjacent to, or stacked with, other equipment. If adja- cent or stacked use is necessary, the IDS2 should be tested to verify normal operation in the con- figuration in which it is being used.
• CW999

  Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the IDS2, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.
• CW999

  Wrong polarity can damage the device! Pay attention to polarity - / +.
• CW999

  Prevent shock-hazard: Never use an IDS2/power supply with damaged housing or ca- ble.
• CW999

  Danger of fatal shock: Use IDS2 in dry environment only. Avoid splashing water. Do not immense in liquids!
• CW999

  Only use original spare parts or accessories.
• CW999

  For separating the connection always pull on the plug, never the cable.

Marché principal en Allemagne ; disponible dans 1 pays au total.

Dénomination commerciale

Isolation Device Server Type II

Code d'UDI-DI

04260346620058

Basic UDI-DI

426034662IDS2rev3XP

Numéro de référence/catalogue

1002Z-IDS-02-BR

Entité d'attribution

GS1

Catégorie de risque

Classe I

Législation applicable

MDR [Règlement (UE) 2017/745 relatif aux dispositifs médicaux]

Statut

Sur le marché

Quantité

1

Description complémentaire du produit

—

URL des informations complémentaires

Aucune URL d'informations complémentaires renseignée par le fabricant.

Dimensions cliniques

Aucune dimension clinique enregistrée pour ce dispositif.

• Z12080180PRENATAL DIAGNOSTIC INSTRUMENTS - HARDWARE ACCESSORIES

• Numéro de lot
• Date d'expiration
• Date de fabrication
• Numéro de série
• Identification du logiciel