PhotonGuide 104008

GUDID 00816728021650

Illuminator, Narrow/Flat

STRYKER CORPORATION

Fibreoptic operating light system

• Primary Device ID: 00816728021650
• NIH Device Record Key: 4685c3f0-d5db-41e6-8b32-3b6084da7e79
• Commercial Distribution Discontinuation: 2022-07-25
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: PhotonGuide
• Version Model Number: Narrow / Flat
• Catalog Number: 104008
• Company DUNS: 196548481
• Company Name: STRYKER CORPORATION
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com
• Phone: +0118002533210
• Email: inst.stryker.cs@stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816728021650 [Primary]

FDA Product Code

• FSZ: Light, Surgical, Carrier

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 7
• Public Version Date: 2022-10-06
• Device Publish Date: 2019-06-03

Devices Manufactured by STRYKER CORPORATION

• 07613327262995 - XIA II: 2025-07-17 CORONAL BENDER LEFT
• 07613327263015 - XIA II: 2025-07-17 CORONAL BENDER RIGHT
• 07613327661989 - KNOTILUS+: 2025-06-24 2.9X15.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE
• 07613327661996 - KNOTILUS+: 2025-06-24 2.4X8.9MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE
• 07613327662009 - KNOTILUS+: 2025-06-24 2.4X11.3MM KNOTILUS+ ANCHOR - BIOCOMPOSITE
• 07613327662016 - KNOTILUS+: 2025-06-24 2.9X12.5MM KNOTILUS+ HIP ANCHOR - BIOCOMPOSITE
• 07613327662023 - KNOTILUS+: 2025-06-24 2.9X12.5MM KNOTILUS+ ANCHOR - BIOCOMPOSITE
• 07613327662030 - ALPHAVENT: 2025-06-24 ALPHAVENT KNOTLESS SP, 4.75MM, BIOCOMPOSITE ANCHOR