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Manufacturers
Megadyne Medical Products, Inc
Manufacturer Address
Megadyne Medical Products, Inc, 11506 South State Street, Draper UT 84020
Source
USFDA
2 Events
Recall of Device Recall Electrosurgery cautery tip
Recall of Device Recall Electrosurgery cautery tip
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2 devices in the database
Device Recall Electrosurgery cautery tip
Model / Serial
Catalog Number 0600M. Lots 00994, 01880, 01181, 01112, 10156, 10670, 11008, 11388, 20260, 20814.
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide. Foreign distribution to Australia, Belgium, Canada, Italy, Korea, New Zealand, Sweden.
Product Description
Megadyne MegaTip, Modified E-Z Clean Non Stick Cautery Tip, CAT/REF 0600M, Single Use Only, STERILE
Device Recall Electrosurgery cautery tip
Model / Serial
Catalog Number 0600. Lots 00664, 00845, 10038, 10190, 10541, 10669, 10703, 10766, 10951, 11110, 11356, 20046, 20219, 20520, 20592, 20757, 20777, 20856, 20997, 21075.
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide. Foreign distribution to Australia, Belgium, Canada, Italy, Korea, New Zealand, Sweden.
Product Description
Megadyne MegaTip, E-Z Clean Non Stick Cautery Tip, CAT/REF 0600, Single Use Only, STERILE
6 manufacturers with a similar name
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Megadyne Medical Products, Inc.
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
NIDFSINVIMA
Megadyne Medical Products, Inc.
Manufacturer Address
Megadyne Medical Products, Inc., 11506 South State Street, Draper UT 84020-9453
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA
Megadyne Medical Products, Inc
Manufacturer Address
Megadyne Medical Products, Inc, 11506 S State St, Draper UT 84020-9453
Source
USFDA
Megadyne Medical Products, Inc
Manufacturer Parent Company (2017)
Megadyne Medical Products, Inc.
Source
SATP
Megadyne Medical Products, Inc.
Manufacturer Address
Megadyne Medical Products, Inc., 11506 S State St, Draper UT 84020-9453
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA
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