Carolon CAP - Carolon Company

Duns Number:061789731

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More Product Details

Catalog Number

551

Brand Name

Carolon CAP

Version/Model Number

Knee

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Safe

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

DWO

Product Code Name

Needle, Biopsy, Cardiovascular

Device Record Status

Public Device Record Key

9756bbec-79b5-4c41-bfbc-cf76aa2816cb

Public Version Date

May 18, 2022

Public Version Number

1

DI Record Publish Date

May 10, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CAROLON COMPANY" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 528
2 A medical device with a moderate to high risk that requires special controls. 39