Spirotome - The Spirotome Biopsy Needle Set is a family of - Bioncise

Duns Number:371402316

Device Description: The Spirotome Biopsy Needle Set is a family of core soft tissue biopsy medical devices to The Spirotome Biopsy Needle Set is a family of core soft tissue biopsy medical devices to be used in humans to take out adequate samples of soft tissue from subdermal structures as breast, abdominal wall, thoracic wall, lymph nodes, thyroid, parotis, muscles, and liver.The Spirotome Biopsy Needle Set contains:• A two-part introducer needle that consists of a cutting cannula and a trocar stylet• A helical-tip receiving needle that has been sized to fit through the lumen of the cutting cannula• A release elementThis presentation has an external diameter of 08G (5mm) and length of 100 mm.

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More Product Details

Catalog Number

SS0810

Brand Name

Spirotome

Version/Model Number

SS0810

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Conditional

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"

Yes

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

K080095,K080095

Product Code Details

Product Code

KNW

Product Code Name

Instrument, Biopsy

Device Record Status

Public Device Record Key

7b6d0bf5-403a-4bca-a99b-896398e2dc5b

Public Version Date

October 01, 2018

Public Version Number

1

DI Record Publish Date

August 31, 2018

Additional Identifiers

Package DI Number

05407005000038

Quantity per Package

5

Contains DI Package

05407005001035

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"BIONCISE" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 22