Pneumosure 0620-040-610

GUDID 07613327063295

XL High Flow Insufflator

STRYKER CORPORATION

Laparoscopic insufflator

• Primary Device ID: 07613327063295
• NIH Device Record Key: d4668090-333a-4036-ac62-64e0ca229ee6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pneumosure
• Version Model Number: 0620040610
• Catalog Number: 0620-040-610
• Company DUNS: 187502109
• 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(866)624-4422
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327063295 [Primary]

FDA Product Code

• HIF: INSUFFLATOR, LAPAROSCOPIC

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

On-Brand Devices [Pneumosure]

• 07613327063295: XL High Flow Insufflator
• 07613327063219: High Flow Insufflator
• 37613327055659: [High Flow Insufflator, Do not use if package is damaged, Keep dry, Keep away from sunlight,
• 37613327055642: [High Flow Insufflator, Do not use if package is damaged, Keep dry, Keep away from sunlight,
• 37613327055635: [High Flow Insufflator, Do not use if package is damaged, Keep dry, Keep away from sunlight,
• 07613327147964: [Tubeset Adapter for PNEUMO SURE High Flow Insufflator. Do Not Use if Package is Damaged, Keep