STORZ 20400162S

GUDID 00628725004365

HIGH FLOW INSUFFLATION TUBING WITH FILTER

Canadian Hospital Specialties Limited

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• Primary Device ID: 00628725004365
• NIH Device Record Key: 6f4948be-278d-44d5-abf0-09f3f5c24caf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STORZ
• Version Model Number: 20400162S
• Catalog Number: 20400162S
• Company DUNS: 240992693
• Company Name: Canadian Hospital Specialties Limited
• 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: false
• Expiration Date: false
• 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	00628725004365 [Primary]
GS1	50628725004360 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• HIF: Insufflator, Laparoscopic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-10

On-Brand Devices [STORZ]

• 00628725004365: HIGH FLOW INSUFFLATION TUBING WITH FILTER
• 00628725004358: HIGH FLOW INSUFFLATION TUBING WITH FILTER