| Primary Device ID | 50833224001196 |
| NIH Device Record Key | 8ded44bd-4c96-4f6f-bc3e-fae34274ee46 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hybrid |
| Version Model Number | HYB535 |
| Catalog Number | HYB535 |
| Company DUNS | 103307950 |
| Company Name | Innomed Technologies Inc |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 800-200-9842 |
| customerservice@innomedinc.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00833224001191 [Primary] |
| GS1 | 50833224001196 [Package] Contains: 00833224001191 Package: [30 Units] In Commercial Distribution |
| BZD | Ventilator, Non-Continuous (Respirator) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-15 |
| 50833224001196 | Hybrid Frame System - LG |
| 50833224001189 | Hybrid Frame System - MD |
| 50833224001172 | Hybrid Frame System - SM |
| 50833224001165 | Hybrid Frame System - All Sizes Kit |
| 50833224000236 | Hybrid SLV Face Mask – All Sizes Kit |
| 50833224000212 | Hybrid Pillows - SM |
| 50833224000205 | Hybrid Pillows - MD |
| 50833224000199 | Hybrid Pillows - LG |
| 50833224000182 | Hybrid Cushion- SM |
| 50833224000175 | Hybrid Cushion- MD |
| 50833224000168 | Hybrid Cushion- LG |
| 50833224000151 | Hybrid Face Mask - All Sizes Kit |