Connected OR OS 0240-060-145

GUDID 07613327311846

STRYKER CORPORATION

Operating room audiovisual data/device management system application software
Primary Device ID07613327311846
NIH Device Record Key7bdf125d-71ff-466f-b4d6-cf47f7a55096
Commercial Distribution StatusIn Commercial Distribution
Brand NameConnected OR OS
Version Model Number0240060145
Catalog Number0240-060-145
Company DUNS187502109
Company NameSTRYKER CORPORATION
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

Phone+1(866)624-4422
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327311846 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRXArthroscope

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-06-30

Devices Manufactured by STRYKER CORPORATION

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07613327648522 - Surpass Elite2025-03-17 Flow Diverter System
07613327648539 - Surpass Elite2025-03-17 Flow Diverter System
07613327648546 - Surpass Elite2025-03-17 Flow Diverter System
07613327648553 - Surpass Elite2025-03-17 Flow Diverter System
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