VanishPoint® - 21G x 3/4" w/7" tubing VanishPoint® Blood - RETRACTABLE TECHNOLOGIES, INC.

Duns Number:838024255

Device Description: 21G x 3/4" w/7" tubing VanishPoint® Blood Collection Set

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More Product Details

Catalog Number

24031

Brand Name

VanishPoint®

Version/Model Number

24031

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Device Record Status

Public Device Record Key

93208115-23f9-4629-b34b-30ab58b060b1

Public Version Date

April 07, 2021

Public Version Number

3

DI Record Publish Date

September 22, 2016

Additional Identifiers

Package DI Number

00613703240323

Quantity per Package

4

Contains DI Package

00613703240316

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case

"RETRACTABLE TECHNOLOGIES, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 77