Celeris

GUDID 00821925044906

DISP SINUS DEBRIDER, 2MM STRT, BIP, TYPE A

Gyrus Acmi, Inc.

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• Primary Device ID: 00821925044906
• NIH Device Record Key: f2a75651-6495-4e6a-9d2a-ba8549b22bd5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Celeris
• Version Model Number: DSD2000BA
• Company DUNS: 007198742
• Company Name: Gyrus Acmi, Inc.
• Device Count: 5
• 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	00821925044906 [Unit of Use]
GS1	00821925044913 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K212650

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-02-18
• Device Publish Date: 2022-02-10

On-Brand Devices [Celeris]

• 00821925045163: DISP SINUS DEBRIDER, 4MM MALL, STD, SERRATED
• 00821925044944: DISP SINUS DEBRIDER, REUSABLE PWR PACK
• 00821925044906: DISP SINUS DEBRIDER, 2MM STRT, BIP, TYPE A
• 00821925044883: DISP SINUS DEBRIDER, 4MM STRT, BIP, TYPE A
• 00821925044876: DISP SINUS DEBRIDER, 4MM STRT, STD, TYPE A