À propos de cette base de données
Comment utiliser cette base de données
Téléchargez les données
FAQ
Crédits
Devices
Device Recall Catheter, Intravascular
Modèle / numéro de série
Lot/Batch Numbers: 23F15L0662,23F15J0260,23F15K0983,23F15G0159,23F15J1102,23F15J0259 23F15C1225,23S15G0973,23F15H1033,23F15F0358,23F15K0345,23F15D1514 23F15C1226,23F15H0919,23F15E1091,23F15H0014,23F15D0241,23F15J0533 23F15E1094,23F15H0020,23F15H0740,23F15K1009,23F15J0431,23F15F1836 23F15H0857,23F15K0012,23F15M0313,23F15G0871,23F15J0285
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
US Distribution to states of: NC, OH, FL, and MD.
Description du dispositif
Cather, Ultrasound, Intravascular || The VPS Stylet and Console are indicated for guidance and tip positioning for central venous catheters.
Manufacturer
Arrow International Inc
2 Events
Rappel de Device Recall Catheter, Intravascular
Rappel de Device Recall Catheter, Intravascular
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
Fabricant
Arrow International Inc
Adresse du fabricant
Arrow International Inc, 2400 Bernville Rd, Reading PA 19605-9607
Société-mère du fabricant (2017)
Teleflex Incorporated
Source
USFDA
Un dispositif médical avec un nom similaire
En savoir plus sur les données
ici
Device Recall Catheter, Intravascular, Therapeutic, ShortTerm
Modèle / numéro de série
Lot/Batch Numbers: 23F15L0662,23F15J0260,23F15K0983,23F15G0159,23F15J1102,23F15J0259 23F15C1225,23S15G0973,23F15H1033,23F15F0358,23F15K0345,23F15D1514 23F15C1226,23F15H0919,23F15E1091,23F15H0014,23F15D0241,23F15J0533 23F15E1094,23F15H0020,23F15H0740,23F15K1009,23F15J0431,23F15F1836 23F15H0857,23F15K0012,23F15M0313,23F15G0871,23F15J0285
Classification du dispositif
General Hospital and Personal Use Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
US Distribution to states of: NC, OH, FL, and MD.
Description du dispositif
Catheter, Intravascular, Therapeutic, Short-Term Less than 30 days || The Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access.
Manufacturer
Arrow International Inc
Language
English
Français
Español
한국어