Catalog Number

CT2200

Brand Name

Crystal Tip

Version/Model Number

CT2200

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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"

-

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

ECB

Product Code Name

UNIT, SYRINGE, AIR AND/OR WATER

Public Device Record Key

0f865a4a-fd2a-4f92-8496-e383b6caf569

Public Version Date

October 31, 2022

Public Version Number

1

DI Record Publish Date

October 23, 2022

Package DI Number

20843471132702

Quantity per Package

6

Contains DI Package

10843471132705

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case