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FAQ
Crédits
Devices
Device Recall Intuiitve Surgical da Vinci EndoWrist
Modèle / numéro de série
FDA Device Listing Number R100529, Model Number 400178-01. 510(k) number K021036.
Classification du dispositif
General and Plastic Surgery Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
The product was distributed to 84 medical facilities, located throughout the US and Switzerland, Belgium, Germany, Australia, Turkey and France.
Description du dispositif
Intuiitve Surgical da Vinci 8 mm EndoWrist Curved Scissors, in box. All lots. P/N 400178-01
Manufacturer
Intuitive Surgical, Inc.
1 Event
Rappel de Device Recall Intuiitve Surgical da Vinci EndoWrist
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Fabricant
Intuitive Surgical, Inc.
Adresse du fabricant
Intuitive Surgical, Inc., 950 Kifer Rd, Sunnyvale CA 94086-5206
Source
USFDA
Language
English
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