Primary Device ID | 00705928003002 |
NIH Device Record Key | fd159c36-768b-4854-8852-cb1673894237 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NeilMed Sinus Rinse |
Version Model Number | Pediatric, 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 | true |
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 | 00705928003002 [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 | 2023-03-10 |
Device Publish Date | 2023-03-02 |
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 |