Catalog Number

-

Brand Name

Avalign

Version/Model Number

VM59-2693

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

-

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

-

Product Code

FHN

Product Code Name

Ligator, Hemorrhoidal

Public Device Record Key

5f52bbb3-393e-4aec-8292-1c7a3dd2d9d7

Public Version Date

July 16, 2018

Public Version Number

1

DI Record Publish Date

June 14, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-