MollRing Cutter Transection Device 4200-40

GUDID 00840663102693

MollRing Cutter Transection Device, 5mm

LEMAITRE VASCULAR, INC.

Intraluminal artery stripper, reusable
Primary Device ID00840663102693
NIH Device Record Keye36299f9-17a6-4348-93f6-86b74e500657
Commercial Distribution StatusIn Commercial Distribution
Brand NameMollRing Cutter Transection Device
Version Model Number4200-40
Catalog Number4200-40
Company DUNS184805166
Company NameLEMAITRE VASCULAR, 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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com
Phone781-221-2266
Emailcsus@lemaitre.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100840663102693 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DWXStripper, Artery, Intraluminal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-07-15

On-Brand Devices [MollRing Cutter Transection Device]

00840663102747MollRing Cutter Transection Device, 10mm
00840663102730MollRing Cutter Transection Device, 9mm
00840663102723MollRing Cutter Transection Device, 8mm
00840663102716MollRing Cutter Transection Device, 7mm
00840663102709MollRing Cutter Transection Device, 6mm
00840663102693MollRing Cutter Transection Device, 5mm

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