Primary Device ID | G51025470 |
NIH Device Record Key | 1a4baa2f-09b1-4ced-b860-84843b3a8024 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GENESIS |
Version Model Number | 2547 |
Company DUNS | 075058495 |
Company Name | Light Sources, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | G51025470 [Primary] |
LEJ | Booth, Sun Tan |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-25 |
Device Publish Date | 2024-06-17 |
G51031560 | 3156 |
G51031900 | 3190 |
G51026520 | 2652 |
G51032410 | 3241 |
G51030940 | 3094 |
G51030460 | 3046 |
G51011850 | 1185 |
G51030450 | 3045 |
G51031980 | 3198 |
G51031890 | 3189 |
G51031620 | 3162 |
G51031580 | 3158 |
G51031570 | 3157 |
G51024840 | 2484 |
G51011660 | 1166 |
G51030930 | 3093 |
G51032200 | 3220 |
G51032000 | 3200 |
G51031990 | 3199 |
G51031600 | 3160 |
G51031590 | 3159 |
G51030300 | 3030 |
G51025630 | 2563 |
G51014000 | 1400 |
G51025600 | 2560 |
G51011890 | 1189 |
G51030800 | 3080 |
G51027720 | 2772 |
G51012870 | 1287 |
G51026590 | 2659 |
G51010320 | 1032 |
G51014460 | 1446 |
G51025610 | 2561 |
G51025470 | 2547 |
G51032530 | 3253 |
G51032250 | 3225 |
G51032240 | 3224 |
G51032010 | 3201 |