CURETTE - KLS-Martin L.P.

Duns Number:826499238

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More Product Details

Catalog Number

-

Brand Name

CURETTE

Version/Model Number

00-102-88-07

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"

-

For Single-Use

-

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

-

Product Code Details

Product Code

FZS

Product Code Name

CURETTE, SURGICAL, GENERAL USE

Device Record Status

Public Device Record Key

a036190b-7502-4906-857f-928c1b3e5f0d

Public Version Date

August 21, 2019

Public Version Number

4

DI Record Publish Date

September 26, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"KLS-MARTIN L.P." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 7013
2 A medical device with a moderate to high risk that requires special controls. 4618