DIEGO IRRIGATION TUBE SET FOR USE WITH VIPER HANDPIECES 12'(3.66 m)

GUDID 00821925027268

Gyrus Acmi, Inc.

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• Primary Device ID: 00821925027268
• NIH Device Record Key: 6a6777f2-f239-4928-ba93-2a76076bce5d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DIEGO IRRIGATION TUBE SET FOR USE WITH VIPER HANDPIECES 12'(3.66 m)
• Version Model Number: 70336900
• Company DUNS: 007198742
• Company Name: Gyrus Acmi, Inc.
• 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: 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
GS1	00821925027268 [Package]; Contains: 00821925040519; Package: [6 Units]; In Commercial Distribution
GS1	00821925040519 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K020594

FDA Product Code

• ERL: DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-05-11