Triton Canister System

GUDID 10859506006101

Box of 50 PN 11033

STRYKER CORPORATION

Blood loss estimation canister insert/label

• Primary Device ID: 10859506006101
• NIH Device Record Key: 1ea91a9a-56d7-4785-b15e-0fd6ebfc1a15
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Triton Canister System
• Version Model Number: FG-12009
• Company DUNS: 196548481
• Company Name: STRYKER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10859506006101 [Primary]

FDA Product Code

• PBZ: Image Processing Device For Estimation Of External Blood Loss

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-06-05
• Device Publish Date: 2018-02-16

On-Brand Devices [Triton Canister System]

• 10859506006132: Box of 50 PN 11035
• 10859506006101: Box of 50 PN 11033
• 10859506006040: Box of 50 PN 11026
• 10859506006033: Box of 50 PN 11015
• 10859506006019: Box of 50 PN 11004