| Primary Device ID | 07290114060899 |
| NIH Device Record Key | 160d8981-5baf-49ca-8d13-08500cd90c51 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Autoclavable Drive |
| Version Model Number | Rev. 4 |
| Catalog Number | 750-000027-00 |
| Company DUNS | 531856466 |
| Company Name | ALPHA OMEGA ENGINEERING CO. LTD. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | 07290114060899 [Primary] |
| GZL | Electrode, Depth |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
[07290114060899]
Dry Heat Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-02-15 |
| Device Publish Date | 2021-02-05 |
| 07290114060899 | Rev. 4 |
| 07290114063296 | Autoclavable Drive |