| Primary Device ID | 00816589020915 |
| NIH Device Record Key | 55110440-8af1-4e50-9ea6-343b495f1eb9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NeuroBlate Optic SideFire® Laser Probe |
| Version Model Number | 20891-3 |
| Catalog Number | NBP-301-01 |
| Company DUNS | 021415875 |
| Company Name | MONTERIS MEDICAL INC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| 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 |
| Phone | +1(866)799-7655 |
| gglaser@monteris.com | |
| Phone | +1(866)799-7655 |
| gglaser@monteris.com | |
| Phone | +1(866)799-7655 |
| gglaser@monteris.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816589020915 [Primary] |
| GEX | Powered laser surgical instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-11-19 |
| Device Publish Date | 2018-10-17 |
| 00816589020939 | 3.3mm Directional Laser Probe |
| 00816589020922 | 3.3mm Directional Laser Probe |
| 00816589020915 | 3.3mm Directional Laser Probe |
| 00816589020908 | 3.3mm Directional Laser Probe |
| 00816589020892 | 3.3mm Directional Laser Probe |
| 00816589020885 | 3.3mm Directional Laser Probe |
| 00816589020878 | 3.3mm Directional Laser Probe |