Catalog Number

08000

Brand Name

flora

Version/Model Number

08000

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

October 04, 2099

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"

-

For Single-Use

-

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

IXY

Product Code Name

Holder, Radiographic Cassette, Wall-Mounted

Public Device Record Key

90c3ac08-cc9f-48a5-b5f7-922afaad240b

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

November 17, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-