Humidx
GUDID 00619498388103
Humidx 6PK
RESMED LIMITED
Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger, single-use Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter Heat/moisture exchanger insertable filter| Primary Device ID | 00619498388103 |
| NIH Device Record Key | 9a637bd1-94ec-4b5d-ad45-c7a5ff87a3ab |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Humidx |
| Version Model Number | 38810 |
| Company DUNS | 751149311 |
| Company Name | RESMED LIMITED |
| 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 | true |
| 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 |
Customer Support Contacts
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com | |
| Phone | 800-427-0737 |
| reception@resmed.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00619498388103 [Primary] |
FDA Product Code
| BYD | Condenser, Heat And Moisture (Artificial Nose) |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-04-29 |
On-Brand Devices [Humidx]
| 00619498388103 | Humidx 6PK |
| 00619498388097 | HumidX 3PK |
| 00619498388080 | Pack of 50 |
Trademark Results [Humidx]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HUMIDX 87284290 5625057 Live/Registered |
RESMED PTY LTD 2016-12-29 |
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