Primary Device ID | 00810026181689 |
NIH Device Record Key | 5cc0fcd5-ac43-489f-8743-ba21e0852213 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RF Generator |
Version Model Number | IEC6-SENSV120 |
Catalog Number | IEC6-SENSV120 |
Company DUNS | 117308190 |
Company Name | SONIQUENCE, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810026181689 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-04-04 |
Device Publish Date | 2020-05-19 |
00810026181931 | RF Generator |
00810026181733 | RF Generator |
00810026181726 | RF Generator |
00810026181719 | RF Generator |
00810026181702 | RF Generator |
00810026181696 | RF Generator |
00810026181689 | RF Generator |
00810026181672 | RF Generator |
00810026181665 | RF Generator |
00810026181658 | RF Generator |
00810026181641 | RF Generator |
00810026181634 | RF Generator |
00810026181627 | RF Generator |
00810026181610 | RF Generator |
00810026181603 | RF Generator |
00810026181597 | RF Generator |
00810026181580 | RF Generator |
00810026181573 | RF Generator |
00810026181566 | RF Generator |
00810026181559 | RF Generator |
00810026181542 | RF Generator |
00810026181535 | RF Generator |