CESSYS®

GUDID 04250337114697

CESSYS® Dorsal FHD Laminoscope (4.7 WCh), combo

Joimax GmbH

Spinal endoscopic-access system
Primary Device ID04250337114697
NIH Device Record Key5fd56f7d-b6dd-4ece-8b5b-a589c8052a6b
Commercial Distribution StatusIn Commercial Distribution
Brand NameCESSYS®
Version Model NumberLS7347068C
Company DUNS344267187
Company NameJoimax 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 Batchfalse
Serial Numbertrue
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

Phone+49721255140
Emailquality@joimax.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104250337114697 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRXArthroscope

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04250337114697]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number2
Public Version Date2018-07-06
Device Publish Date2018-03-08

On-Brand Devices [CESSYS®]

04250337114697CESSYS® Dorsal FHD Laminoscope (4.7 WCh), combo
04250337114680CESSYS® Dorsal FHD Laminoscope (4.7 WCh), ocular
04250337105879CESSYS® Cervical Hybrid Scope, combo
04250337116837CESSYS® Dorsal DIN-Norm-Container, yellow Lid
04250337108818CESSYS® DIN-Norm-Container, gold Lid
04250337105152CESSYS® Cervical Reamer

Trademark Results [CESSYS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CESSYS
CESSYS
79062669 3799655 Live/Registered
joimax GmbH
2008-10-10

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