Catalog Number

MK72AE102

Brand Name

EXMOOR

Version/Model Number

MK/72/A/E102

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

JYP

Product Code Name

Knife, Myringotomy

Public Device Record Key

e8afb9f2-2c04-4746-a1b1-c41e953cdc06

Public Version Date

May 10, 2019

Public Version Number

2

DI Record Publish Date

October 08, 2018

Package DI Number

05060180253240

Quantity per Package

10

Contains DI Package

05060180252434

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

a box