Primary Device ID | 00810096330017 |
NIH Device Record Key | f2555d38-f3ea-499b-98b6-fb1df7d08ad1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Digital Duet™ |
Version Model Number | Digital Duet™ |
Company DUNS | 118292380 |
Company Name | Lumenis Be, 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 | 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 | 00810096330017 [Primary] |
HQF | Laser, Ophthalmic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-22 |
Device Publish Date | 2023-05-12 |
00810096330000 - Selecta Duet™ | 2023-05-22 |
00810096330017 - Digital Duet™ | 2023-05-22 |
00810096330017 - Digital Duet™ | 2023-05-22 |
00810096330024 - Smart-V Illumination Add-on | 2023-05-22 |
00810096330062 - Smart532 | 2023-04-10 |
00810096330079 - Array LaserLink | 2023-04-10 |
00810096330086 - Vision One | 2023-04-10 |
00810096330093 - Vision One | 2023-04-10 |
00810096330109 - Vision One | 2023-04-10 |