Primary Device ID | 72990012704126 |
NIH Device Record Key | f24cf516-1be0-475b-a5e5-72a825113bb7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BeamMed |
Version Model Number | PLATFORM FORCE-MEASURING |
Company DUNS | 534155155 |
Company Name | BEAMMED LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | true |
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 | 72990012704126 [Primary] |
KHX | Platform, Force-Measuring |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-09-05 |
Device Publish Date | 2017-01-25 |
07299012704119 | "Omnisense 7000: The Sunlight Omnisense Ultrasound Bone Sonometer is a non-invasive ultrasound d |
07290012704109 | "Sunlight MiniOmni: The Sunlight MiniOmni Ultrasound Bone Sonometer is a non-invasive ultrasound |
72990012704126 | "Tetrax balance assessment is used to quantitatively detect changes in postural responses that h |