Standard 64 Tip,Fuse (200 Puls), Steril, SubRF AS74876

GUDID 07290109950624

Standard 64 Tip,Fuse (200 Puls), Steril, SubRF

SYNERON MEDICAL LTD

Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system

• Primary Device ID: 07290109950624
• NIH Device Record Key: 36a7b951-113a-48d5-ad08-61a185ca4ff7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Standard 64 Tip,Fuse (200 Puls), Steril, SubRF
• Version Model Number: AS74876
• Catalog Number: AS74876
• Company DUNS: 532685716
• Company Name: SYNERON MEDICAL 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109950624 [Primary]
GS1	37290109950625 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090025

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2018-07-06
• Device Publish Date: 2016-09-26

Devices Manufactured by SYNERON MEDICAL LTD

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• 07290109952857 - Intima Sterile 2 Internal + 1 External HP, Accessories Kit: 2020-02-10 Intima Sterile 2 Internal + 1 External HP, Accessories Kit
• 07290109952864 - eTwo System: 2020-02-10 eTwo System
• 17290109952724 - Regular Internal Handpiece 5-Pack Sterile Single-Use, CO2RE Intima: 2020-02-10 Regular Internal Handpiece 5-Pack Sterile Single-Use, CO2RE Intima
• 17290109952823 - External Handpiece 5-Pack Sterile Single-Use, CO2RE Intima: 2020-02-10 External Handpiece 5-Pack Sterile Single-Use, CO2RE Intima
• 17290109950379 - Internal, CO2RE Intima: 2019-02-07 Internal, CO2RE Intima
• 07290109950167 - Purple swivel lens: 2019-02-07 Purple swivel lens
• 07290109950273 - Lens, Gold & Silver: 2019-02-07 Lens, Gold & Silver Assy, CO2RE