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Crédits
Manufacturers
Wright Medical Technology, Inc.
Adresse du fabricant
Wright Medical Technology, Inc., 1023 Cherry Rd, Memphis TN 38117-5423
Société-mère du fabricant (2017)
Wright Medical Group NV
Source
USFDA
34 Events
Rappel de Device Recall CLAW(R) II STRAIGHT PLATE ORTHOLOC(TM) 3DSi, LENGTH 25mm x 25mm
Rappel de Device Recall CLAW(R) II STRAIGHT PLATE ORTHOLOC(TM) 3DSi, LENGTH 20mm x 25mm
Rappel de Device Recall CLAW(R) II STRAIGHT PLATE ORTHOLOC(TM) 3DSi, LENGTH 20mm x 20mm
Rappel de Device Recall CLAW(R) II 2 HOLE PLATE ORTHOLOC(TM) 3DSi, LENGTH 30mm
Rappel de Device Recall CLAW(R) II 2 HOLE PLATE ORTHOLOC(TM) 3DSi, LENGTH 25mm
Rappel de Device Recall CLAW(R) II 2 HOLE PLATE ORTHOLOC(TM) 3DSi, LENGTH 20mm
Rappel de Device Recall CLAW(R) II 2 HOLE PLATE ORTHOLOC(TM) 3DSi, LENGTH 15mm
Rappel de Device Recall CLAW(R) 3.5mm PLATE CHARLOTTE(R) F&A; SYSTEM, SIZE 30mm, 2 HOLE
Rappel de Device Recall CLAW(R) PLATE 20mm INTERAXIS CHARLOTTE(R) F&A; SYSTEM
Rappel de PHALINX (TM) HAMMERTOE HANDLE, SIZE: LARGE, STYLE: ANGLED, REF 45304014
Rappel de PHALINX (TM) HAMMERTOE HANDLE, SIZE: MEDIUM, STYLE: ANGLED, REF 45304013
Rappel de PHALINX (TM) HAMMERTOE HANDLE, SIZE: SMALL, STYLE: ANGLED, REF 45304012
Rappel de PHALINX (TM) HAMMERTOE HANDLE, SIZE: XSMALL, STYLE: ANGLED, REF 45304011
Rappel de Device Recall CrossCHECK Locking Screw
Rappel de Device Recall CrossCHECK Locking Screw
Rappel de Device Recall CROSSCHECK(R) Plating system, YPLATE CX, REF CCPYPX1
Rappel de Device Recall CROSSCHECK(R) Plating system, Utility Plate, 7Hole, REF CCPUTN7
Rappel de Device Recall CROSSCHECK(R) Plating system, Utility Plate, 6Hole, REF CCPUTN6
Rappel de Device Recall CROSSCHECK(R) Plating system, Utility Plate, 5Hole, REF CCPUTN5
Rappel de Device Recall CROSSCHECK(R) Plating system, Utility Plate, 4Hole, REF CCPUTN4
Rappel de Device Recall CROSSCHECK(R) Plating system, Utility Plate, 3Hole, REF CCPUTN3
Rappel de Device Recall CROSSCHECK(R) Plating system, Utility Plate, 2Hole, REF CCPUTN2
Rappel de Device Recall CROSSCHECK(R) Plating system, MTP CX Plate, Right, REF CCPMPX1R
Rappel de Device Recall CROSSCHECK(R) Plating system, MTP CX Plate, Left, REF CCPMPX1L
Rappel de Device Recall CROSSCHECK(R) Plating system, MTP NX Plate, Right, Recon, REF CCPMPN2R
Rappel de Device Recall CROSSCHECK(R) Plating system, MTP NX Plate, Left, Recon, REF CCPMPN2L
Rappel de Device Recall CROSSCHECK(R) Plating system, LAPIDUS CX plate, 2mm Step, Right, REF CCPLPX2R
Rappel de Device Recall CROSSCHECK(R) Plating system, LAPIDUS CX Plate, 2mm Step, Left, REF CCPLPX2L
Rappel de Device Recall CROSSCHECK(R) Plating system, LAPIDUS CX Plate, 1mm Step, Right, REF CCPLPX1R
Rappel de Device Recall CROSSCHECK(R) Plating system, LAPIDUS CX Plate, 1mm Step, Left, REF CCPLPX1L
Rappel de Device Recall CROSSCHECK(R) Plating system, LAPIDUS CX Plate, NEUTRAL, Right, REF CCPLPX0R
Rappel de Device Recall CROSSCHECK(R) Plating system, LAPIDUS CX Plate, NEUTRAL, Left, REF CCPLPX0L
Rappel de Device Recall CROSSCHECK(R) Plating system, HOCKEY STICK CX Plate, Right, REF CCPHSX1R
Rappel de Device Recall CROSSCHECK(R) Plating system, HOCKEY STICK CX Plate, Left, REF CCPHSX1L
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34 dispositifs dans la base de données
Device Recall CLAW(R) II STRAIGHT PLATE ORTHOLOC(TM) 3DSi, LENGTH 25mm x 25mm
Modèle / numéro de série
Lot Numbers: 1517327, 1538333, 1543490
Classification du dispositif
Orthopedic Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.
Description du dispositif
CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 25mm x 25mm, REF 40242525, 1 EACH, Rx ONLY, NON STERILE || Orthopedic
Device Recall CLAW(R) II STRAIGHT PLATE ORTHOLOC(TM) 3DSi, LENGTH 20mm x 25mm
Modèle / numéro de série
Lot Numbers: 1513144, 1518479, 1534798, 1538331, 1543489
Classification du dispositif
Orthopedic Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.
Description du dispositif
CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 20mm x 25mm, REF 40242025, 1 EACH, Rx ONLY, NON STERILE || Orthopedic
Device Recall CLAW(R) II STRAIGHT PLATE ORTHOLOC(TM) 3DSi, LENGTH 20mm x 20mm
Modèle / numéro de série
Lot Numbers: 1512153, 1518480, 1532497, 1538075, 1538076, 1538332
Classification du dispositif
Orthopedic Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.
Description du dispositif
CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 20mm x 20mm, REF 40242020, 1 EACH, Rx ONLY, NON STERILE || Orthopedic
Device Recall CLAW(R) II 2 HOLE PLATE ORTHOLOC(TM) 3DSi, LENGTH 30mm
Modèle / numéro de série
Lot Numbers: 1487670, 1487671, 1487672, 1512149, 1519496, 1523745, 1534796, 1537159, 1539400, 1540714
Classification du dispositif
Orthopedic Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.
Description du dispositif
CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 30mm, REF 40240230, 1 EACH, Rx ONLY, NON STERILE || Orthopedic
Device Recall CLAW(R) II 2 HOLE PLATE ORTHOLOC(TM) 3DSi, LENGTH 25mm
Modèle / numéro de série
Lot Numbers: 1490367, 1490368, 1512152, 1521232, 1523734, 1523746, 1537160, 1537161, 1539401, 1541613, 1541614, 1542652, 1542774, 1542775
Classification du dispositif
Orthopedic Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.
Description du dispositif
CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 25mm, REF 40240225, 1 EACH, Rx ONLY, NON STERILE || Orthopedic
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Wright Medical Technology, Inc.
Adresse du fabricant
Wright Medical Technology, Inc., 11576 Memphis Arlington Rd, Arlington TN 38002-9497
Société-mère du fabricant (2017)
Wright Medical Group NV
Source
USFDA
Wright Medical Brasil Ltda Me; Wright Medical Technology, Inc.
Société-mère du fabricant (2017)
Wright Medical Group NV
Source
ANVSANVISA
Wright Medical Technology, Inc.
Société-mère du fabricant (2017)
Wright Medical Group NV
Source
DMA
Language
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