| Primary Device ID | 00705928001008 |
| NIH Device Record Key | 42a430f9-1b9e-44d1-a7eb-702803d0b090 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NeilMed Sinus Rinse |
| Version Model Number | NeilMed Sinus Rinse Kit 60 Premixed Sachets |
| Company DUNS | 799295915 |
| Company Name | NEILMED PHARMACEUTICALS, 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 | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00705928001008 [Primary] |
| KCJ | Applicator, Ent |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-25 |
| Device Publish Date | 2022-10-17 |
| 00705928001008 | Sinus Rinse products contain pre-weighed and sealed salt-soda mixture packets/sachets. The Kit v |
| 00705928003002 | Sinus Rinse products contain pre-weighed and sealed salt-soda mixture packets/sachets. The Kit v |
| 00705928002043 | Sinus Rinse products contain pre-weighed and sealed salt-soda mixture packets/sachets. The Kit v |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEILMED SINUS RINSE 87703337 5668378 Live/Registered |
NEILMED PHARMACEUTICALS, INC. 2017-11-30 |