Catalog Number

-

Brand Name

Dialator Nettle Ship

Version/Model Number

90-1012

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

HNW

Product Code Name

Dilator, Lachrymal

Public Device Record Key

c7ce3a07-99e1-4a4d-8ab9-f2c0c3f6ca5a

Public Version Date

July 08, 2022

Public Version Number

1

DI Record Publish Date

June 30, 2022

Package DI Number

05060480402447

Quantity per Package

10

Contains DI Package

05060480407947

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-