CEREBASE GS9080SD

GUDID 10886704082316

CEREBASE DA Guide Sheath Working Length: 80 cm ID: 0.090 in/2.29 mm Short Sheath Compatability: 8F

Medos International Sàrl

Vascular guide-catheter, single-use

• Primary Device ID: 10886704082316
• NIH Device Record Key: af287b1d-0bdd-415d-8546-64f6625fbd87
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CEREBASE
• Version Model Number: GS9080SD
• Catalog Number: GS9080SD
• Company DUNS: 482661753
• Company Name: Medos International Sàrl
• Device Count: 1
• DM Exempt: true
• 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: true
• 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(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886704082316 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192804

FDA Product Code

• QJP: Catheter, Percutaneous, Neurovasculature

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-21
• Device Publish Date: 2020-04-13

On-Brand Devices [CEREBASE]

• 10886704082323: CEREBASE DA Guide Sheath Working Length: 95 cm ID: 0.090 in/2.29 mm Short Sheath Compatability:
• 10886704082316: CEREBASE DA Guide Sheath Working Length: 80 cm ID: 0.090 in/2.29 mm Short Sheath Compatability:
• 10886704082309: CEREBASE DA Guide Sheath Working Length: 70 cm ID: 0.090 in/2.29 mm Short Sheath Compatability:
• 10886704082293: CEREBASE DA Guide Sheath Working Length: 90 cm ID: 0.090 in/2.29 mm Short Sheath Compatability: