Primary Device ID | 10840277403145 |
NIH Device Record Key | 380a13f5-4d3d-43c2-a63d-9998ad05b139 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MedLED Onyx Sapphire |
Version Model Number | M-90002 |
Company DUNS | 964053560 |
Company Name | RIVERPOINT MEDICAL, LLC |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840277403148 [Primary] |
GS1 | 10840277403145 [Package] Contains: 00840277403148 Package: [2 Units] In Commercial Distribution |
HPP | Headlamp, Operating, Battery-Operated |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-06 |
Device Publish Date | 2023-11-28 |
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