Nasal probe Starter Kit

GUDID 07290109141312

Additional DM DIs: 07290109144337 07290109144344 07290109144351 07290109144368 07290109144375 07290109144382 07290109144399 07290109144405 07290109144412

LUMENIS LTD.

General/multiple surgical solid-state/carbon dioxide laser system Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor Laser adaptor

• Primary Device ID: 07290109141312
• NIH Device Record Key: 0f1abed6-1313-477b-babd-e8c9b14e0980
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nasal probe Starter Kit
• Version Model Number: 14630
• 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: true
• Serial Number: false
• Manufacturing Date: false
• 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	07290109141312 [Primary]
GS1	07290109144320 [Direct Marking]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

Sterilization

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

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

Moist Heat or Steam Sterilization

[07290109141312]

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: 2016-08-25

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• 07290109147062 - VersaPulse PowerSuite 80/100W: 2022-09-27