| Primary Device ID | 10328785201069 |
| NIH Device Record Key | 91eccf33-a027-475a-9a8d-0d42e0e3c6bc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kaz |
| Version Model Number | 4100-HF |
| Company DUNS | 001483890 |
| Company Name | KAZ, INC. |
| Device Count | 1 |
| 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 | false |
| 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 | 00328785201062 [Primary] |
| GS1 | 10328785201069 [Package] Contains: 00328785201062 Package: Case [6 Units] In Commercial Distribution |
| KFZ | Humidifier, Non-Direct Patient Interface (Home-Use) |
| 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 | 2017-11-30 |
| 10328785221005 | VAPORIZER,1GL,N/L,6-PACK |
| 10328785201069 | HUMIDIFIER, HOSPITAL, 4100 |
| 10328785001478 | HUMIDIFIER, IMPELLER,1 GL. |
| 10328785000457 | Thermometer, Clear, Digital |