Reprocessed 4mm EndoScrub Sheath, 45 deg, K Storz

GUDID B39019120131

SURETEK MEDICAL

Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter

• Primary Device ID: B39019120131
• NIH Device Record Key: 3eb871f0-f8e5-427b-be28-8bf924a17be9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed 4mm EndoScrub Sheath, 45 deg, K Storz
• Version Model Number: 19-12013
• Company DUNS: 785616934
• Company Name: SURETEK MEDICAL
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B39019120131 [Primary]

FDA Product Code

• KAM: Cannula, Sinus

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: 2021-06-23
• Device Publish Date: 2021-06-15

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