Twister XXL 101315-IC

GUDID 00859337007028

lateral emitting laser fiber

WISDOM MEDICAL TECHNOLOGY, LLC

General/multiple surgical laser system beam guide, reusable
Primary Device ID00859337007028
NIH Device Record Key38127487-b97b-40c3-ba95-3110fcb6a493
Commercial Distribution StatusIn Commercial Distribution
Brand NameTwister XXL
Version Model Number101315-IC
Catalog Number101315-IC
Company DUNS080537625
Company NameWISDOM MEDICAL TECHNOLOGY, LLC
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

Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net
Phone630-803-6383
Emailjfurcht@verizon.net

Device Identifiers

Device Issuing AgencyDevice ID
GS100859337007028 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-07-06
Device Publish Date2017-10-02

On-Brand Devices [Twister XXL]

00869851000337lateral emitting laser fiber
00859337007028lateral emitting laser fiber

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