PlasmaBladeTM

GUDID 00643169507869

PLASMABLADE PS210-030S 3.0S LOCK

MEDTRONIC, INC.

Open-surgery electrosurgical handpiece/electrode, monopolar, single-use
Primary Device ID00643169507869
NIH Device Record Key46ee5f17-b2d3-4f98-ae9f-367f7a2258bc
Commercial Distribution StatusIn Commercial Distribution
Brand NamePlasmaBladeTM
Version Model NumberPS210-030S
Company DUNS030200852
Company NameMEDTRONIC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169507869 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-02-07
Device Publish Date2016-04-16

On-Brand Devices [PlasmaBladeTM]

00643169616820PLASMABLADE PS200-040-SP 4.0
00643169616813PLASMABLADE PS200-040 4.0 PINK
00643169531024PLASMABLADE PS210-030P PLUS LOCK
00643169531017PLASMABLADE PS210-030S PINK LOCK
00643169507869PLASMABLADE PS210-030S 3.0S LOCK
00643169491915PLASMABLADE PS200-040 4.0
00643169456235PLASMABLADE PS300-006 PEAK UPPP ENT

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.