Primary Device ID | 07290015461498 |
NIH Device Record Key | fc26b5be-b788-4dda-b60c-8ef37f08867e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ExAblate 2100 LOWER PELVIC COIL ASSEMBLY |
Version Model Number | ASM000506-AA ExAblate 2100 LOWER PELVIC COIL ASSEM |
Catalog Number | ASM000506-AA |
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 | 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 |
Phone | 18663922528 |
info@insightec.com |
Storage Environment Temperature | Between -15 Degrees Celsius and 55 Degrees Celsius |
Storage Environment Temperature | Between -15 Degrees Celsius and 55 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290015461498 [Primary] |
NRZ | Ablation System, High Intensity Focused Ultrasound (Hifu), Mr-Guided |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2018-11-29 |
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