J & J INSTRUMENTS INC - ACORN BURNISHER DE #21B - J & J INSTRUMENTS INC

Duns Number:783328149

Device Description: ACORN BURNISHER DE #21B

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

02-600

Brand Name

J & J INSTRUMENTS INC

Version/Model Number

02-600

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)

-

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

EKJ

Product Code Name

Burnisher, Operative

Device Record Status

Public Device Record Key

aa69dc0c-1fae-41c6-94bc-52f48b7bb94e

Public Version Date

November 19, 2018

Public Version Number

1

DI Record Publish Date

October 17, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"J & J INSTRUMENTS INC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 840
2 A medical device with a moderate to high risk that requires special controls. 6