Reprocessed 4.0mm Hummer IV Aggressive Cutter

GUDID B39052906480001

Reprocessed Hummer IV 4.0mm Aggressive Cutter, 8cm

SURETEK MEDICAL

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• Primary Device ID: B39052906480001
• NIH Device Record Key: 4772ef08-e950-4546-b079-f737e33f8f4c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reprocessed 4.0mm Hummer IV Aggressive Cutter
• Version Model Number: 5290-648-000
• 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	B39052906480001 [Primary]

FDA Product Code

• NBH: Accessories, Arthroscopic

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: 2021-06-23
• Device Publish Date: 2019-05-15

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