Aveta Max+ Disposable Resecting Device, 3.9 mm 210-2013

GUDID 10850006759726

Aveta Max+ Disposable Resecting Device, 3.9 mm, for use with Aveta System

MEDITRINA, INC.

Tissue morcellation system handpiece, line-powered

• Primary Device ID: 10850006759726
• NIH Device Record Key: 063204ff-b623-468d-875c-865defb641df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aveta Max+ Disposable Resecting Device, 3.9 mm
• Version Model Number: 210-2013
• Catalog Number: 210-2013
• Company DUNS: 080570262
• Company Name: MEDITRINA, 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	00850006759729 [Primary]
GS1	10850006759726 [Package]; Contains: 00850006759729; Package: Shelf carton [3 Units]; In Commercial Distribution

FDA Product Code

• HIG: Insufflator, Hysteroscopic

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: 2023-12-11
• Device Publish Date: 2023-12-01

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• 10850006759726 - Aveta Max+ Disposable Resecting Device, 3.9 mm: 2023-12-11Aveta Max+ Disposable Resecting Device, 3.9 mm, for use with Aveta System
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