Catalog Number

00-0764-002-10

Brand Name

N/A

Version/Model Number

00-0764-002-10

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"

Yes

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

ILI

Product Code Name

Sling, Arm

Public Device Record Key

b6ca9c1e-f295-4939-a2cc-5a43ae3b2e51

Public Version Date

September 29, 2020

Public Version Number

1

DI Record Publish Date

September 21, 2020

Package DI Number

00889024378483

Quantity per Package

10

Contains DI Package

00889024368453

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box