Twister XL 101300

GUDID 00869851000320

lateral emitting laser fiber

WISDOM MEDICAL TECHNOLOGY, LLC

General/multiple surgical laser system beam guide, reusable
Primary Device ID00869851000320
NIH Device Record Keyf6c70242-dbdd-497b-ae41-2b0d19a97e07
Commercial Distribution StatusIn Commercial Distribution
Brand NameTwister XL
Version Model Number101300
Catalog Number101300
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
GS100869851000320 [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 Date2017-06-20

On-Brand Devices [Twister XL]

00869851000320lateral emitting laser fiber
00859337007042lateral emitting laser fiber

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