| Primary Device ID | 10328785835028 |
| NIH Device Record Key | b3d81533-27bd-46ea-a78c-ca7b1e536903 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PROTEC |
| Version Model Number | PWF2 |
| Company DUNS | 001483890 |
| Company Name | KAZ, INC. |
| Device Count | 3 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | 800-477-0457 |
| consumerrelations@kaz.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00328785835021 [Primary] |
| GS1 | 10328785835028 [Package] Contains: 00328785835021 Package: CASE [6 Units] In Commercial Distribution |
| GS1 | 20328785835025 [Unit of Use] |
| KFZ | Humidifier, Non-Direct Patient Interface (Home-Use) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-10-01 |
| Device Publish Date | 2018-08-31 |
| 10328785835028 | HUMIDIFIER FILTER, WICKING, WF2, PROTEC |
| 50328785808136 | FILTER, WICKING, WF813, PROTEC |
| 10328785001560 | PROTEC Humidifier Filter Clip Strip of 4 PWF2 |
| 00092926083007 | PROTEC, WICKING HUMIDIFIER FILTER, PACK FOR AMAZON |