NeilMed Sinus Rinse - Sinus Rinse products contain pre-weighed and - NEILMED PHARMACEUTICALS, INC.

Duns Number:799295915

Device Description: Sinus Rinse products contain pre-weighed and sealed salt-soda mixture packets/sachets. The Sinus Rinse products contain pre-weighed and sealed salt-soda mixture packets/sachets. The Kit variants also contain a bottle assembly (bottle, cap and tube that is affixed to the cap). The packets/sachets contain a defined ratio of sodium chloride and sodium bicarbonate that provides a pH balanced isotonic, solution the resulting saline solution is squirted through a bottle assembly designed at NeilMed Products, Inc.The regular Isotonic Sinus Rinse packets/sachets have salt concentration with a tonicity close to that of plasma or serum. The Isotonic Sinus Rinse Kit comes with a 240mL bottle premixed Packets/sachets containing a mixture of sodium chloride and sodium bicarbonate. This produces 0.9 % saline solution on mixing one packet with 240mL of water. The packets/sachets also come in an individual box.

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More Product Details

Catalog Number

-

Brand Name

NeilMed Sinus Rinse

Version/Model Number

NeilMed Sinus Rinse Kit 60 Premixed Sachets

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

KCJ

Product Code Name

Applicator, Ent

Device Record Status

Public Device Record Key

42a430f9-1b9e-44d1-a7eb-702803d0b090

Public Version Date

October 25, 2022

Public Version Number

1

DI Record Publish Date

October 17, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"NEILMED PHARMACEUTICALS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 3
U Unclassified 1