Connect OR OS 0240-060-140

GUDID 07613327311839

STRYKER CORPORATION

Operating room audiovisual data/device management system application software
Primary Device ID07613327311839
NIH Device Record Keye290a20f-d314-4a8f-9877-296bd0e70b2b
Commercial Distribution StatusIn Commercial Distribution
Brand NameConnect OR OS
Version Model Number0240060140
Catalog Number0240-060-140
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
GS107613327311839 [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

07613327163278 - NA2025-04-28
07613327601138 - OptaBlate2025-04-25 Curve 10mm Probe Single Kit
07613327601145 - OptaBlate2025-04-25 Curve 20mm Probe Single Kit
07613327601152 - OptaBlate2025-04-25 Curve 15mm Probe Single Kit
07613327631883 - OptaBlate2025-04-25 Straight 10MM Probe Dual Kit
07613327631890 - OptaBlate2025-04-25 Straight 10MM Probe Single Kit
07613327626391 - ThermaClear2025-04-14
07613327626407 - ThermaClear2025-04-14

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.