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FAQ
Crédits
Devices
Device Recall The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM),
Modèle / numéro de série
All Schiller PB-1000 PDM's distributed on or before 8/11/2016.
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Distribution US nationwide.
Description du dispositif
The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM), a major component of the Merge Hemo software.
Manufacturer
Merge Healthcare, Inc.
1 Event
Rappel de Device Recall The Schiller PB 1000, also known as Merge Hemo Patient Data Module (PDM),
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Fabricant
Merge Healthcare, Inc.
Adresse du fabricant
Merge Healthcare, Inc., 900 Walnut Ridge Dr, Hartland WI 53029-8347
Société-mère du fabricant (2017)
International Business Machines Corp.
Source
USFDA
Language
English
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