TruDi NAV Suction - TruDi NAV Suction, 90° - 1PK - ACCLARENT, INC.

Duns Number:361092450

Device Description: TruDi NAV Suction, 90° - 1PK

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More Product Details

Catalog Number

TDNS090Z

Brand Name

TruDi NAV Suction

Version/Model Number

TDNS090Z

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Unsafe

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

K180948,K180948

Product Code Details

Product Code

PGW

Product Code Name

Ear, Nose, and Throat Stereotaxic Instrument

Device Record Status

Public Device Record Key

5ea3f347-de97-4fe3-a406-353fc4d906c8

Public Version Date

January 22, 2020

Public Version Number

2

DI Record Publish Date

January 20, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ACCLARENT, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 83
2 A medical device with a moderate to high risk that requires special controls. 43