Catalog Number

1638502

Brand Name

Sapphire

Version/Model Number

1638502

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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"

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

MRZ

Product Code Name

ACCESSORIES, PUMP, INFUSION

Public Device Record Key

65a67a2e-cdec-4ba1-a66c-37e7a4145d43

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

January 31, 2017

Package DI Number

20887787006500

Quantity per Package

50

Contains DI Package

10887787006503

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case