AcuSpot 712 L Micromanipulator

GUDID 07290109141916

Additional DM DIs: 07290109144290 07290109144313

LUMENIS LTD.

General/multiple surgical solid-state/carbon dioxide laser system ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator ENT surgery micromanipulator

• Primary Device ID: 07290109141916
• NIH Device Record Key: a3922030-7638-4d84-9bbc-c22b4a71afdd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AcuSpot 712 L Micromanipulator
• Version Model Number: AcuSpot 712 L Micromanipulator
• Company DUNS: 600166524
• Company Name: LUMENIS LTD.
• 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: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109141916 [Primary]
GS1	07290109144306 [Direct Marking]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

Sterilization

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

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

[07290109141916]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-04-29
• Device Publish Date: 2016-09-13

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