Primary Device ID | 00812444029048 |
NIH Device Record Key | d6ca228b-0ff5-4dda-8755-e8ac218f4ef0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MedLED Classic |
Version Model Number | ML001-SK |
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 | 00812444029048 [Primary] |
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 | 2024-04-26 |
Device Publish Date | 2024-04-18 |
10840277405798 - Umbilical Tape | 2024-10-16 Tape |
10840277405804 - Umbilical Tape | 2024-10-16 Tape |
10840277405811 - Umbilical Tape | 2024-10-16 Tape |
00840277404923 - HS Fiber | 2024-10-10 Suture |
00840277402974 - RibFix Titan | 2024-09-02 60mm Extrathoracic Pre-Bent Plate, Non-Sterile, Plate: Titanium |
00840277402981 - RibFix Titan | 2024-09-02 94mm Extrathoracic Pre-Bent Plate, Non-Sterile, Plate: Titanium |
00840277402998 - RibFix Titan | 2024-09-02 120mm Extrathoracic Pre-Bent Plate, Non-Sterile, Plate: Titanium |
00840277403001 - RibFix Titan | 2024-09-02 60mm Intrathoracic Pre-Bent Plate, Non-Sterile, Plate: Titanium |