Trimedyne® R-50™ Spinal Introduction Cannula 70052

GUDID M473700521

Introducer, Spine, 1.75mm ID

TRIMEDYNE, INC.

Arthroscopic access cannula, single-use

• Primary Device ID: M473700521
• NIH Device Record Key: f88183fe-ceb5-4f2e-bda9-77266d59670c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trimedyne® R-50™ Spinal Introduction Cannula
• Version Model Number: 70052
• Catalog Number: 70052
• Company DUNS: 057007239
• Company Name: TRIMEDYNE, 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

Customer Support Contacts

• Phone: 8007335273
• Email: customerservice@trimedyne.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M473700520 [Primary]
HIBCC	M473700521 [Package]; Contains: M473700520; Package: Carton [5 Units]; In Commercial Distribution

FDA Product Code

• BSP: Needle, Conduction, Anesthetic (W/Wo Introducer)

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: 2020-02-27
• Device Publish Date: 2018-07-11

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