Versacut™ GA-0000200

GUDID 07290109146904

Versacut Tissue Morcellator, MORCELLATOR WITH HOLEP TRAINING

LUMENIS LTD.

Tissue morcellation system
Primary Device ID07290109146904
NIH Device Record Key2cc6ed89-715f-48c1-8587-ba04e1a691ec
Commercial Distribution StatusIn Commercial Distribution
Brand NameVersacut™
Version Model NumberVersacut™
Catalog NumberGA-0000200
Company DUNS600166524
Company NameLUMENIS LTD.
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 Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107290109146904 [Primary]

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-12
Device Publish Date2022-09-04

On-Brand Devices [Versacut™]

07290109143095Steralization Tray
07290109146904Versacut Tissue Morcellator, MORCELLATOR WITH HOLEP TRAINING
07290109146850VersaCut Tissue Morcellator Control Unit

Trademark Results [Versacut]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VERSACUT
VERSACUT
90788038 not registered Live/Pending
Exmark Manufacturing Company Incorporated
2021-06-22
VERSACUT
VERSACUT
87164884 not registered Dead/Abandoned
Blount, Inc.
2016-09-08
VERSACUT
VERSACUT
85337728 4083771 Live/Registered
Positec Group Limited
2011-06-03
VERSACUT
VERSACUT
78891915 3220085 Live/Registered
Makino Inc.
2006-05-24
VERSACUT
VERSACUT
75708442 2468327 Dead/Cancelled
CardioThoracic Systems, Inc.
1999-05-18
VERSACUT
VERSACUT
73029655 1030571 Dead/Expired
FAIRFIELD MACHINE COMPANY, INC.
1974-08-15

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