AP410-01 - SECONDARY INFUSION SET WITH VENTED/NONVENTED DRIP CHAMBER - Q-CORE MEDICAL LTD

Duns Number:533108028

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More Product Details

Catalog Number

12005-000-0007

Brand Name

AP410-01 - SECONDARY INFUSION SET WITH VENTED/NONVENTED DRIP CHAMBER

Version/Model Number

12005-000-0007

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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

K123049,K123049

Product Code Details

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Device Record Status

Public Device Record Key

9ab5fc5e-b404-4f8f-a180-a55490df3514

Public Version Date

June 25, 2019

Public Version Number

1

DI Record Publish Date

June 17, 2019

Additional Identifiers

Package DI Number

27290109159229

Quantity per Package

30

Contains DI Package

17290109159222

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