Kalitec Disc Prep - Rasp, Angled Lumbar - Kalitec Direct LLC

Duns Number:041956211

Device Description: Rasp, Angled Lumbar

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More Product Details

Catalog Number

DR-K01-0027

Brand Name

Kalitec Disc Prep

Version/Model Number

DR-K01-0027

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

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

HTR

Product Code Name

Rasp

Device Record Status

Public Device Record Key

77e1d3ac-5440-4948-8bae-a3da2c68c4d6

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

June 15, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"KALITEC DIRECT LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1286
2 A medical device with a moderate to high risk that requires special controls. 1900