AP410-01- SECONDARY INFUSION SET WITH VENTED/NON-VENTED DRIP CHAMBER, ROLLER CLA - 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/NON-VENTED DRIP CHAMBER, ROLLER CLA

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

K192860,K192860

Product Code Details

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Device Record Status

Public Device Record Key

de5d3ef4-606f-4c6e-b7c5-ec2ad72cad42

Public Version Date

May 23, 2022

Public Version Number

1

DI Record Publish Date

May 15, 2022

Additional Identifiers

Package DI Number

27290109153159

Quantity per Package

30

Contains DI Package

17290109153152

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