Primary Device ID | 07290109140513 |
NIH Device Record Key | 1b50d50a-ffa0-4b2f-9864-346c62eae3c9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lumenis Pulse 120H |
Version Model Number | Lumenis Pulse 120H |
Company DUNS | 600166524 |
Company Name | LUMENIS 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 | 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 | 408-764-3000 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290109140513 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-15 |
Device Publish Date | 2016-08-23 |
07290109140513 | Lumenis Pulse 120H |
07290109145525 | Lumenis Pulse Moses 2.0 (DOM) |
07290109145518 | Lumenis Pulse P120 30 Amp |
07290109145501 | Lumenis Pulse 120H |
07290109145495 | Lumenis Pulse 120H |
07290109145488 | Lumenis Pulse 120H |
07290109145464 | Lumenis Pulse 120H |
07290109145457 | Lumenis Pulse 120H |
07290109145440 | Lumenis Pulse 120H |
07290109145433 | Lumenis Pulse 120H |
07290109145426 | Lumenis Pulse 120H |
07290109145419 | Lumenis Pulse 120H |
07290109145402 | Lumenis Pulse 120H |
07290109145150 | Lumenis Pulse Moses 2.0(INT) |