microTargeting™ Insertion Tube - microTargeting Single Electrode Insertion Tube - FHC, INC.

Duns Number:108179458

Device Description: microTargeting Single Electrode Insertion Tube Set, Sterile, for use with Nexframe and Nex microTargeting Single Electrode Insertion Tube Set, Sterile, for use with Nexframe and Nexdrive. Contains: IT(DB3): Insertion Tube - 191.6mm tube length, 1.83mm od, 1.6mm idPT(DB3): Protective Tube - 0.58mm id

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More Product Details

Catalog Number

66-IT-4000

Brand Name

microTargeting™ Insertion Tube

Version/Model Number

66-IT-4000-00370

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

Yes

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

K011775,K011775

Product Code Details

Product Code

HAW

Product Code Name

Neurological stereotaxic Instrument

Device Record Status

Public Device Record Key

34080b28-dd49-4308-86ee-218687ba76fb

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 17, 2016

Additional Identifiers

Package DI Number

10873263003708

Quantity per Package

5

Contains DI Package

00873263003701

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

PK/5

"FHC, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 4
2 A medical device with a moderate to high risk that requires special controls. 476