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Crédits
Manufacturers
Applied Medical Resources Corp
Adresse du fabricant
Applied Medical Resources Corp, 22872 Avenida Empresa, Rancho Santa Margarita CA 92688
Société-mère du fabricant (2017)
Applied Medical Corporation
Source
USFDA
7 Events
Rappel de Device Recall Lap Banding Kit
Rappel de Device Recall Lap Banding Kit
Rappel de Device Recall Lap Banding Kit
Rappel de Device Recall 15mm Separator Access System
Rappel de Device Recall 15mm Separator Access System
Rappel de Device Recall 15mm Separator Access System
Rappel de Device Recall 15mm Separator Access System
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7 dispositifs dans la base de données
Device Recall Lap Banding Kit
Modèle / numéro de série
Product/Kit Batch Numbers: 1059636, 1060354, 1061309, 1062314
Classification du dispositif
General and Plastic Surgery Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide and Canada distribution.
Description du dispositif
Applied Medical, Lap Roux-EN-Y Kit, REF: K2129 Contains: (1) C0Q04, 5x100mm Threaded Kii Access System (1) C0130, 12x100mm Optical Separator System, Non-handled || (2) C0Q10, 5x100mm Threaded Kii Cannula and Seal (1) C0605, 15mmx100mm Threaded Cannula System, for laparoscopic procedures.
Device Recall Lap Banding Kit
Modèle / numéro de série
Product/Kit Batch Numbers: 1059718, 1060488, 1061516, 1062296, 1063810
Classification du dispositif
General and Plastic Surgery Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide and Canada distribution.
Description du dispositif
Applied Medical, Lap Banding Kit, REF: K0406 Contains: (1) C0658, 11x100mm Threaded Shielded Trocar w/Universal Seal (1) C0522, 5x100mm Threaded Premium Flat Blade (1) C2202, 150mm Insufflation needle (1) C0605, 15x100mm Threaded Separator Access System (1) CB030, 5mm x 35cm Direct Drive Disposable Scissors (2) C4120, 5mm x 38cm Direct Drive Grasper Reposable Cartridge, for laparoscopic procedures.
Device Recall Lap Banding Kit
Modèle / numéro de série
Product/Kit Batch Numbers: 1057269, 1057814, 1058172, 1058834, 1059466, 1059823, 1060637, 1061254, 1062450, 1062867, 1063561, 1063797, 1064872
Classification du dispositif
General and Plastic Surgery Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide and Canada distribution.
Description du dispositif
Applied Medical, Lap Banding Kit, REF: K0398 Contains: (2) C0Q04, 5x100mm Threaded Kii Access System (1) C0604, 15x100mm Non-Threaded Separator System w/Universal Seal, for laparoscopic procedures.
Device Recall 15mm Separator Access System
Modèle / numéro de série
Product/Kit Batch Numbers: 1060178, 1056644, 1056045
Classification du dispositif
Obstetrical and Gynecological Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide and Canada distribution.
Description du dispositif
Applied Medical, Separator Abdominal Access System REF: C0607 15x150mm Threaded Separator System with Universal Seal, for laparoscopic procedures.
Device Recall 15mm Separator Access System
Modèle / numéro de série
Product/Kit Batch Number 1059804
Classification du dispositif
Obstetrical and Gynecological Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide and Canada distribution.
Description du dispositif
Applied Medical, Separator Abdominal Access System REF: C0606 15x150mm Non-threaded Separator System with Universal Seal, for laparoscopic procedures.
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Applied Medical Resources Corporation
Société-mère du fabricant (2017)
Applied Medical Corporation
Source
NZMMDSA
Applied Medical Resources Corp.
Société-mère du fabricant (2017)
Applied Medical Corporation
Source
LAANSM
Applied Medical Resources Corp
Adresse du fabricant
Applied Medical Resources Corp, 22872 Avenida Empresa, Rancho Santa Margarita CA 92688-2650
Société-mère du fabricant (2017)
Applied Medical Corporation
Source
USFDA
Applied Medical Resources Corporation
Société-mère du fabricant (2017)
Applied Medical Corporation
Source
BAM
Applied Medical Resources Corp
Adresse du fabricant
Applied Medical Resources Corp, 22872 Avenida Empresa # 3, Rancho Santa Margarita CA 92688-2650
Société-mère du fabricant (2017)
Applied Medical Corporation
Source
USFDA
4 en plus
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