Primary Device ID | 10328785001478 |
NIH Device Record Key | a0ffe146-4ddb-4ca7-8cf9-383f6ca90f75 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kaz |
Version Model Number | 4100 |
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 | 00328785001471 [Primary] |
GS1 | 10328785001478 [Package] Contains: 00328785001471 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 | 2017-11-03 |
10328785221005 | VAPORIZER,1GL,N/L,6-PACK |
10328785201069 | HUMIDIFIER, HOSPITAL, 4100 |
10328785001478 | HUMIDIFIER, IMPELLER,1 GL. |
10328785000457 | Thermometer, Clear, Digital |