In-Light Camera P59109

GUDID 07613327661194

STRYKER COMMUNICATIONS INC.

Surgical video camera
Primary Device ID07613327661194
NIH Device Record Keycc01153c-b304-42af-bcf6-7db311d6787c
Commercial Distribution StatusIn Commercial Distribution
Brand NameIn-Light Camera
Version Model NumberP59109
Catalog NumberP59109
Company DUNS078807493
Company NameSTRYKER COMMUNICATIONS INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com
Phone+1(866)726-3705
EmailSCC-CS2@stryker.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327661194 [Primary]

FDA Product Code

KQMCAMERA, SURGICAL AND ACCESSORIES

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-09-04
Device Publish Date2025-08-27

Devices Manufactured by STRYKER COMMUNICATIONS INC.

07613327661194 - In-Light Camera2025-09-04
07613327661194 - In-Light Camera2025-09-04
07613327054507 - FLEXIS2023-06-15
07613327589344 - OPERON2022-03-30 Pad Set 20" Leg, W Cutout, 3"
07613327054286 - NA2020-08-06 Suspension, Navigation System, 10'
07613327054293 - NA2020-08-06 Suspension, Navigation System
07613327054514 - NA2020-08-06 Medium-Duty Dual Yoke
07613327054521 - NA2020-08-06 Medium-Duty Suspension
07613327054538 - NA2020-08-06 Light-Duty Suspension

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