Catalog Number

ILLY 182540

Brand Name

ILLY NEEDLE

Version/Model Number

ILLY NEEDLE

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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"

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

K020987,K020987

Product Code

KNW

Product Code Name

Instrument, Biopsy

Public Device Record Key

07cb43fa-246d-4a5f-9ff3-7b4eae5031e5

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

December 04, 2016

Package DI Number

38033055143371

Quantity per Package

10

Contains DI Package

08033055143370

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-