AcuPort Zone Cannulated 8 GA x 200mm 308.087

GUDID 00889024406506

ZIMMER KNEE CREATIONS, INC.

Bone grafting cannula

• Primary Device ID: 00889024406506
• NIH Device Record Key: 32cd7b7f-6e47-4c03-8163-1d9b8d8e0922
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AcuPort Zone Cannulated 8 GA x 200mm
• Version Model Number: 308.087
• Catalog Number: 308.087
• Company DUNS: 078836317
• Company Name: ZIMMER KNEE CREATIONS, INC.
• 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

Customer Support Contacts

• Phone: 484-887-8902
• Email: KC.Customerservice@zimmerbiomet.com

Device Dimensions

• Length: 200 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024406506 [Primary]

FDA Product Code

• FGY: Cannula, Injection

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: 2019-02-07
• Device Publish Date: 2016-05-19

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