MiniFESS Turbinate Forceps - The MiniFESS Turbinate Forceps is a reusable - ENTELLUS MEDICAL, INC.

Duns Number:017283879

Device Description: The MiniFESS Turbinate Forceps is a reusable device used to grasp, manipulate or compress The MiniFESS Turbinate Forceps is a reusable device used to grasp, manipulate or compress tissue in the nasal or sinus cavity.

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More Product Details

Catalog Number

-

Brand Name

MiniFESS Turbinate Forceps

Version/Model Number

CS-101

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

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

KAE

Product Code Name

Forceps, Ent

Device Record Status

Public Device Record Key

4a022939-393b-4a04-bb08-85c659395b36

Public Version Date

September 16, 2020

Public Version Number

1

DI Record Publish Date

September 08, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ENTELLUS MEDICAL, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 22
2 A medical device with a moderate to high risk that requires special controls. 27