Primary Device ID | 07290114064064 |
NIH Device Record Key | 799d735d-b07c-49c9-8a56-56aec1c0afda |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Remote Control |
Version Model Number | Remote Control |
Catalog Number | 750-000032-00 |
Company DUNS | 531856466 |
Company Name | ALPHA OMEGA ENGINEERING CO. LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | 07290114064064 [Primary] |
GZL | Electrode, Depth |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-01-12 |
Device Publish Date | 2022-11-08 |
07290114064033 | Remote Control |
07290114064064 | Remote Control |
07290114064057 | Remote Control |