Catalog Number

E207

Brand Name

EXMOOR

Version/Model Number

E.207

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

K911503,K911503

Product Code

KHJ

Product Code Name

Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material)

Public Device Record Key

4b0cb3ff-1937-4e5e-a3b1-6a579ed51af8

Public Version Date

October 15, 2019

Public Version Number

2

DI Record Publish Date

September 21, 2018

Package DI Number

05060180259242

Quantity per Package

25

Contains DI Package

05060180259235

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

a box