Scar Patch SET000554

GUDID 07290015461108

A single use (disposable) non-invasive non-active medical device intended for contact with the patient’s intact (continuous) skin surface to serve as a barrier for Focused Ultrasound energy of the FUS beam trajectory by covering scar tissues for up to 4 hours, during an ExAblate MRgFUS treatment, and avoid scar over-heating.

INSIGHTEC LTD

Therapeutic oncological/gynaecological ultrasound system

• Primary Device ID: 07290015461108
• NIH Device Record Key: 92abaf08-373d-4e58-a20a-2644625d8914
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Scar Patch
• Version Model Number: Scar Patch for Body
• Catalog Number: SET000554
• Company DUNS: 532169513
• Company Name: INSIGHTEC LTD
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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: 18663922528
• Email: info@insightec.com

Operating and Storage Conditions

• Handling Environment Temperature: Between 10 Degrees Celsius and 40 Degrees Celsius
• Handling Environment Temperature: Between 10 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290015461108 [Primary]

FDA Product Code

• LSY: Ultrasound,Hyperthermia, Cancer Treatment

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-08
• Device Publish Date: 2017-06-07

Devices Manufactured by INSIGHTEC LTD

• 07290019402442 - HEADFRAME PFK TYPE 1.0 FDA/ROW INTEGRA (FMI): 2023-07-04 HEADFRAME PFK TYPE 1.0 FDA/ROW INTEGRA (FMI). Multi use Stereotactic Frame Set for fixing the skull position during neuro FUS cl
• 07290019402466 - HEADFRAME PFK TYPE 1.1 FDA/ROW INTEGRA (FMI): 2023-07-04 HEADFRAME PFK TYPE 1.1 FDA/ROW INTEGRA (FMI). Multi use Stereotactic Frame Set for fixing the skull position during neuro FUS cl
• 07290019402121 - EXABLATE NEURO PATIENT TREATMENT KIT 3.0T SI: 2023-06-22 EXABLATE NEURO PATIENT TREATMENT KIT 3.0T SI w/PFK for 5 treatments for Siemens MR PFK package served ETO-sterile
• 07290019402138 - EXABLATE NEURO PATIENT TREATMENT KIT 3.0T SI SU: 2023-06-22 EXABLATE NEURO PATIENT TREATMENT KIT 3.0T SI w/PFK for 1 treatment for Siemens MR PFK package served ETO-sterile
• 07290019402145 - EXABLATE NEURO PATIENT TREATMENT KIT 1.5T GE: 2023-06-22 EXABLATE NEURO PATIENT TREATMENT KIT 1.5T GE w/PFK for 5 treatments for GE MR PFK package served ETO-sterile
• 07290019402152 - EXABLATE NEURO PATIENT TREATMENT KIT 3.0T SI SU: 2023-06-22 EXABLATE NEURO PATIENT TREATMENT KIT 1.5T GE SU w/PFK for 1 treatment for GE MR PFK package served ETO-sterile
• 07290019402169 - EXABLATE NEURO PATIENT TREATMENT KIT 3.0T GE: 2023-06-22 EXABLATE NEURO PATIENT TREATMENT KIT 3.0T GE w/PFK for 5 treatments for GE MR PFK package served ETO-sterile
• 07290019402176 - EXABLATE NEURO PATIENT TREATMENT KIT 3.0T GE SU: 2023-06-22 EXABLATE NEURO PATIENT TREATMENT KIT 3.0T GE SU w/PFK for 1 treatment for GE MR PFK package served ETO-sterile