StrykeCam P36000

GUDID 07613327488784

For F-Gen

STRYKER COMMUNICATIONS INC.

Surgical video camera

• Primary Device ID: 07613327488784
• NIH Device Record Key: 0ed7f9b2-897d-4b32-9dfa-26e3664aab10
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: StrykeCam
• Version Model Number: P36000
• Catalog Number: P36000
• Company DUNS: 078807493
• Company Name: STRYKER COMMUNICATIONS INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(866)726-3705
• Email: SCC-CS2@stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327488784 [Primary]

FDA Product Code

• KQM: CAMERA, SURGICAL AND ACCESSORIES

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-10-04
• Device Publish Date: 2019-09-26

On-Brand Devices [StrykeCam]

• 07613327488784: For F-Gen
• 07613327502046: For Visum LED