Reprocessed 4mm EndoScrub 2 Sheath, 0 deg, w/Tubing

GUDID B3901912038T1

Reprocessed 4mm Endo-Scrub 2 Sheath, 0 deg, w/Tubing. Used with Olympus WA96200A

SURETEK MEDICAL

Optical medical device procedural cover

• Primary Device ID: B3901912038T1
• NIH Device Record Key: 3eaf3681-3617-45de-892c-da0adedcd51f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed 4mm EndoScrub 2 Sheath, 0 deg, w/Tubing
• Version Model Number: 19-12038T
• 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	B3901912038T1 [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: 2025-05-09
• Device Publish Date: 2025-05-01

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• B3901912038T1 - Reprocessed 4mm EndoScrub 2 Sheath, 0 deg, w/Tubing: 2025-05-09 Reprocessed 4mm Endo-Scrub 2 Sheath, 0 deg, w/Tubing. Used with Olympus WA96200A
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