BIOPSYBELL - KYPHOPLASTY DRILL - BIOPSYBELL SRL

Duns Number:438746708

Device Description: KYPHOPLASTY DRILL

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More Product Details

Catalog Number

RESDRI1112C-US

Brand Name

BIOPSYBELL

Version/Model Number

RENOVA SPINE KYPHOPLASTY DRILL

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"

Yes

For Single-Use

Yes

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

HXY

Product Code Name

Brace, Drill

Device Record Status

Public Device Record Key

a5e113d3-1c8b-4a19-953c-97fd4890e64c

Public Version Date

June 22, 2020

Public Version Number

1

DI Record Publish Date

June 12, 2020

Additional Identifiers

Package DI Number

08033860034801

Quantity per Package

5

Contains DI Package

08033860034771

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BLISTER

"BIOPSYBELL SRL" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 41
2 A medical device with a moderate to high risk that requires special controls. 37