Trimedyne® 1210-VHPA OmniPulse Max™ Holmium Laser System 1210-VHPA

GUDID M4731210VHPA0

Model 1210-VHPA - OmniPulse Max Holmium Laser System

TRIMEDYNE, INC.

General/multiple surgical solid-state laser system

• Primary Device ID: M4731210VHPA0
• NIH Device Record Key: 02a73c4e-506f-40ae-b3b1-37c4a9796027
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trimedyne® 1210-VHPA OmniPulse Max™ Holmium Laser System
• Version Model Number: 1210-VHPA
• Catalog Number: 1210-VHPA
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	M4731210VHPA0 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-02-27
• Device Publish Date: 2018-07-11

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