Catalog Number

040161

Brand Name

BIOMARC ® RESTORE

Version/Model Number

040161

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

IYE

Product Code Name

Accelerator, Linear, Medical

Public Device Record Key

fe34d694-6400-41c8-a77c-5810e72bcb3a

Public Version Date

October 04, 2022

Public Version Number

3

DI Record Publish Date

December 16, 2021

Package DI Number

10850002461159

Quantity per Package

1

Contains DI Package

00850002461152

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CARTON