À propos de cette base de données
Comment utiliser cette base de données
Téléchargez les données
FAQ
Crédits
Manufacturers
Aspen Surgical Products, Inc.
Adresse du fabricant
Aspen Surgical Products, Inc., 6945 Southbelt Dr Se, Caledonia MI 49316-7664
Société-mère du fabricant (2017)
Hill-Rom Holdings, Inc
Source
USFDA
28 Events
Rappel de Device Recall Walcott RX Products Corneal Marking Pad Sterile
Rappel de Device Recall Viscot Corneal Marking Pad, Sterile
Rappel de Device Recall OcuSoft Corneal Marking Oad, Sterile
Rappel de Device Recall Eagle Labs Corneal Marking Pad, Sterile
Rappel de Device Recall Aspen Corneal Marking Pad Sterile
Rappel de Device Recall Oasis Corneal Ink Stamp Sterile
Rappel de Device Recall 7mm Drain Kit Flat 3/4 Perforated with 100ml SVac Bulb Evacuator, Sterile (10/case)
Rappel de Device Recall 7mm Drain Kit Flat Full Perforated with Trocar and 100ml SVac Bulb Evacuator, Sterile (10/case)
Rappel de Device Recall 19FR Drain Kit Flat Full Perforated with Trocar, Saber 100ml Bulb and 3CSystem, Sterile (10/case)
Rappel de Device Recall 15FR Drain Kit Round End Perforated with Trocar and 100ml SVac Bulb Evacuator, Sterile (10/case)
Rappel de Device Recall 10mm Drain Kit Flat Full Perforated with 100ml SVac Bulb Evacuator, Sterile (10/case)
Rappel de Device Recall 7mm Drain Kit Flat Full Perforated with 100ml SVac Bulb Evacuator, Sterile (10/case)
Rappel de Device Recall 10mm Drain Kit Flat 3/4 Perforated with 100ml SVac Bulb Evacuator, Sterile (10/case)
Rappel de Device Recall 10mm Drain Kit Flat Full Perforated with Trocar and 100ml SVac Bulb Evacuator, Sterile (10/case)
Rappel de Device Recall 10mm Drain Kit Flat 3/4 Perforated with Trocar and 100ml SVac Bulb Evacuator, Sterile (10/case)
Rappel de Device Recall 19FR Drain Kit Full Fluted with Trocar and 100ml SVac Bulb, Sterile (10/case)
Rappel de Device Recall 15FR Drain Kit Full Fluted with Trocar and 100ml SVac Bulb, Sterile (10/case)
Rappel de Device Recall 10FR Drain Kit Full Fluted with Trocar and 100ml SVac Bulb, Sterile (10/case)
Rappel de Device Recall 7mm Drain Kit Fluted 4 Channel with 100ml SVac Bulb, Sterile (10/case)
Rappel de Device Recall Saber 100ml Infection Control PVC Bulb Evacuator, Sterile (10/case)
Rappel de Device Recall Saber 100ml Infection Control PVC Bulb with 150ml 3C System, Sterile (10/case)
Rappel de Device Recall 15FR Drain Kit, Flat Full Perforated with Trocar, Saber 100ml Bulb and 3C System, Sterile (10/case)
Rappel de Device Recall 10FR Drain Kit, Flat Full Perforated with Trocar, Saber 100ml Bulb and 3C System, Sterile (10/case)
Rappel de Device Recall 10mm Drain Kit, Flat Full Perforated, Saber 100ml Bulb and 3C System Sterile (10/case)
Rappel de Device Recall 7mm Drain Kit, Flat Full Perforated, Saber 100ml Bulb and 3C System Sterile (10/case)
Rappel de Device Recall Wound Closure Strips
Rappel de Surgidyne SVac round fluted channel silicone drain kit
Rappel de Surgidyne SVac round fluted channel silicone drain
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
28 dispositifs dans la base de données
Device Recall Walcott RX Products Corneal Marking Pad Sterile
Modèle / numéro de série
2013-01-12, 2013-09-13.
Classification du dispositif
Ophthalmic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide distribution including USA Canada, England, Sweden, Saudi Arabia, England, Hong Kong, Belgium and Israel.
Description du dispositif
Walcott Rx Products, Surgical Division, Corneal Marking Pad, REF RX40490, Sterile. For use in ophthalmic surgery.
Device Recall Viscot Corneal Marking Pad, Sterile
Modèle / numéro de série
2010-10-14, 2010-12-02, 2012-02-03, 2012-03-17, 2012-04-14, 2012-06-23, 2012-07-20, 2012-10-12, 2012-11-30, 2013-03-12, 2013-04-08, 2013-04-22, 2013-07-28, 2013-09-01.
Classification du dispositif
Ophthalmic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide distribution including USA Canada, England, Sweden, Saudi Arabia, England, Hong Kong, Belgium and Israel.
Description du dispositif
Viscot Medical, LLC., Vismark Gentian Violet Marking Pad, Rx Only, Sterile, REF GV1200S. For use in ophthalmic surgery.
Device Recall OcuSoft Corneal Marking Oad, Sterile
Modèle / numéro de série
2012-08-24, 2012-10-12, 2012-11-17, 2012-12-15.
Classification du dispositif
Ophthalmic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide distribution including USA Canada, England, Sweden, Saudi Arabia, England, Hong Kong, Belgium and Israel.
Description du dispositif
CYNACON OcuSOFT LASIK Marker Pads, REF 750-093, Rx Only, Sterile. For use in ophthalmic surgery.
Device Recall Eagle Labs Corneal Marking Pad, Sterile
Modèle / numéro de série
2010-12-09, 2013-02-23, 2013-08-12, 2013-09-24.
Classification du dispositif
Ophthalmic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide distribution including USA Canada, England, Sweden, Saudi Arabia, England, Hong Kong, Belgium and Israel.
Description du dispositif
Eagle Labs Corneal Marking Pad, Gentian Violet, REF 63-001, Sterile. For use in ophthalmic surgery.
Device Recall Aspen Corneal Marking Pad Sterile
Modèle / numéro de série
2010-10-07, 2012-10-12, 2012-11-30, 2012-12-15, 2013-04-09, 2013-04-23, 2013-05-21, 2013-09-01, 2013-10-01.
Classification du dispositif
Ophthalmic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide distribution including USA Canada, England, Sweden, Saudi Arabia, England, Hong Kong, Belgium and Israel.
Description du dispositif
Aspen Surgical, Corneal Marking Pad, Gentian Violet Ink, REF 40490, Rx only, Sterile. For use in ophthalmic surgery.
23 en plus
3 fabricants avec un nom similaire
En savoir plus sur les données
ici
Aspen Surgical Products, Inc.
Adresse du fabricant
Aspen Surgical Products, Inc., 7425 Clyde Park Ave Sw Ste G, Byron Center MI 49315-8373
Source
USFDA
Aspen Surgical Products, Inc..
Société-mère du fabricant (2017)
Hill-Rom Holdings, Inc
Représentant du fabricant
Sehat Al-Jazeera EST.
Source
SFDA
Aspen Surgical Products, Inc.
Adresse du fabricant
Aspen Surgical Products, Inc., 7425 Clyde Park SW, Ste. G, Byron Center MI 49315
Source
USFDA
Language
English
Français
Español
한국어