Primary Device ID | 00859729006011 |
NIH Device Record Key | eeffc985-01ae-46c5-b05a-6352056e88ed |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FMX |
Version Model Number | DPM |
Catalog Number | FMDPM |
Company DUNS | 963249342 |
Company Name | DOMAIN SURGICAL, INC. |
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 | 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 | 00859729006011 [Primary] |
GS1 | 10859729006018 [Package] Package: Sterile Pouch [1 Units] In Commercial Distribution |
GS1 | 20859729006015 [Package] Contains: 10859729006018 Package: Box [5 Units] In Commercial Distribution |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-06-08 |
00859729006035 | FMX G1 Generator Foot Pedal |
00859729006028 | FMX Reusable Power Module |
00859729006011 | FMX Disposable Power Module |
00859729006004 | FMX G1 Generator |