SapphirePlus Infusion Kit - US - Q-CORE MEDICAL LTD

Duns Number:533108028

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More Product Details

Catalog Number

17000-033-0001

Brand Name

SapphirePlus Infusion Kit - US

Version/Model Number

17000-033-0001

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K141389,K141389,K141389,K141389

Product Code Details

Product Code

FRN

Product Code Name

Pump, Infusion

Device Record Status

Public Device Record Key

51c959d8-46b7-4db8-889f-a199e6fea371

Public Version Date

July 04, 2022

Public Version Number

5

DI Record Publish Date

February 22, 2018

Additional Identifiers

Package DI Number

27290109150226

Quantity per Package

8

Contains DI Package

17290109150229

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

cardboard box

"Q-CORE MEDICAL LTD" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 65