BLUEENDO 501-040-721

GUDID 04251303822011

Obturator Ø 15 mm for complete system

TROKAMED GmbH

Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable
Primary Device ID04251303822011
NIH Device Record Keya6f8cd98-6f3c-48c6-b0cf-4f45865b27a1
Commercial Distribution StatusIn Commercial Distribution
Brand NameBLUEENDO
Version Model Number55-151006
Catalog Number501-040-721
Company DUNS341943858
Company NameTROKAMED GmbH
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Countertrue

Customer Support Contacts

Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de
Phone+49770492440
Emailsales@trokamed.de

Device Identifiers

Device Issuing AgencyDevice ID
GS104251303822011 [Primary]

FDA Product Code

HETLaparoscope, Gynecologic (And Accessories)

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


[04251303822011]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-01
Device Publish Date2023-02-21

On-Brand Devices [BLUEENDO]

04251303811343Foot Pedal, single
04251303811459Valve Module for Morcellator System, including a reducer Ø 10 - 5 mm, single use, sterile, 5 pc
04251303811442Cutting Module Ø 15 mm to be used with 02-33103, Color Code grey, for Morcellator System, sin
04251303811435Grip Module V2.0, 5-times-use for Morcellator System
04251303811428Grasping Forceps, single action, Ø 10 mm, WL 420 mm, incl. outer tube Ø 13 mm
04251303811411Tenaculum Forceps, jaws Ø 10 mm, double action, Ø 10 mm, WL 420 mm, incl. outer tube Ø 13 mm
04251303811404Tenaculum Forceps, jaws Ø 7 mm, double action, Ø 10 mm, WL 420 mm, incl. outer tube Ø 13 mm
04251303811398Obturator Ø 15 mm for complete system to be used with 02-33103
04251303811381Obturator Ø 15 mm, to be used with 02-33103, Color Code grey
04251303811374Protection Sleeve Ø 15 mm, WL 170 mm, Color Code grey
04251303811367Flexible Shaft, WL 2,5 m
04251303811329Control Unit Morcellator - USA
04251303811350Rinsing Adapter for Grip Module Morcellator
04251303822042Changable outer tube Ø 13mm for forceps Ø 10mm, WL 420 mm
04251303822035Claw grasper forceps Ø 13 / 10mm, jaws Ø 10mm, single action, two teeth, ring handle stainless
04251303822028Obturator Ø 20 mm for complete system
04251303822011Obturator Ø 15 mm for complete system
04251303822004Obturator Ø 12,5 mm for complete system
04251303821991Protection Sleeve Ø 20 mm, WL 120 mm, color code yellow
04251303821984Protection Sleeve Ø 15 mm, WL 120 mm, color code grey
04251303821977Protection Sleeve Ø 12,5 mm, WL 120mm color code green
04251303812074Cutting module Ø 12,5mm for Morcellator System, Color Code green, single-use, sterile, 5 pcs./
04251303812067Cutting module Ø 15 mm short for Morcellator System Release 2, Color Code grey, single-use, st
04251303812043Grip Module V2.0, 5-times-use for Morcellator System
04251303812012Flexible Shaft, WL 2,5 m
04251303811954Tenaculum forceps Ø 13 / 10mm, WL 330mm, jaws Ø 10mm, double action, two teeth, ring handle st
04251303811893Cutting module Ø 20 mm short for Morcellator System Release 2, Color Code yellow, single-use,
04251303811886Valve module Ø 10mm, BlueEndo, for Morcellator System with Reducer Ø 10- 5mm single-use, steri
04251303822103Trocar, conical blunt Ø 20 mm for protective sleeve WL 170 mm color code yellow
04251303822097Trocar, conical blunt Ø 15 mm for protective sleeve WL 170 mm color code grey
04251303822080Trocar, conical blunt Ø 12,5 mm for protective sleeve WL 170 mm color code green

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