Trimedyne® 550 µm Test Laser Fiberoptic 760

GUDID M4737600

Test Fiber, 550um, Holmium

TRIMEDYNE, INC.

General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable General/multiple surgical laser system beam guide, reusable
Primary Device IDM4737600
NIH Device Record Keyd1fe3c2e-15c0-484a-ba8c-cabd496bef80
Commercial Distribution StatusIn Commercial Distribution
Brand NameTrimedyne® 550 µm Test Laser Fiberoptic
Version Model Number760
Catalog Number760
Company DUNS057007239
Company NameTRIMEDYNE, 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 Usefalse
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

Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com
Phone8007335273
Emailcustomerservice@trimedyne.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM4737600 [Primary]

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-02-27
Device Publish Date2018-07-11

Devices Manufactured by TRIMEDYNE, INC.

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M47312100 - Trimedyne® 1210 OmniPulse™ Holmium Laser System2020-02-27 Model 1210 - OmniPulse Holmium Laser System
M4731210VHP0 - Trimedyne® 1210-VHP OmniPulse Max™ Holmium Laser System2020-02-27 Model 1210-VHP - OmniPulse Max Holmium Laser System
M4731210VHPA0 - Trimedyne® 1210-VHPA OmniPulse Max™ Holmium Laser System2020-02-27 Model 1210-VHPA - OmniPulse Max Holmium Laser System
M4731230300 - Trimedyne® 1230-30 OmniPulse Jr.™ Holmium Laser System2020-02-27 Model 1230-30 - OmniPulse Jr. Holmium Laser System
M4731500A0 - Trimedyne® Model 1500-A Holmium Laser System2020-02-27 Model 1500-A - Holmium Laser System
M47320021M0 - Trimedyne® FlexMax® 550 µm Reusable Holmium Bare Fiber2020-02-27 Fiber, Bare, 550um, Reusable, TMED Connector
M47320021MSMA0 - Trimedyne® FlexMax® 550 µm Reusable Holmium Bare Fiber (SMA Connector)2020-02-27 Fiber, Bare, 550um, Reusable, SMA Connector

Trademark Results [Trimedyne]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TRIMEDYNE
TRIMEDYNE
74055774 1636817 Live/Registered
Trimedyne, Inc.
1990-05-04

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