Catalog Number

-

Brand Name

NETCELL

Version/Model Number

10-125T

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 15, 2021

Issuing Agency

In GS1

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LYA

Product Code Name

Splint, Intranasal Septal

Public Device Record Key

91981a50-515c-4694-8ee3-6a105a59f0e2

Public Version Date

December 16, 2021

Public Version Number

4

DI Record Publish Date

August 05, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-