| Primary Device ID | 27290114061111 |
| NIH Device Record Key | 987b968b-c5e3-47e9-83b2-53f4c66fd6fa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Leksell Non-XY frame Mechanical Set KIT |
| Version Model Number | 2 |
| Catalog Number | 700-020832-00 |
| 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 | 27290114061111 [Primary] |
| GZL | Electrode, Depth |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
[27290114061111]
Dry Heat Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-02-25 |
| Device Publish Date | 2021-02-17 |
| 27290114061111 | 2 |
| 27290114064099 | Long Bengun |