Geistlich Bio-Oss® - Geistlich Pharma AG

Duns Number:480781728

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More Product Details

Catalog Number

-

Brand Name

Geistlich Bio-Oss®

Version/Model Number

500804

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

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

NPM

Product Code Name

Bone Grafting Material, Animal Source

Device Record Status

Public Device Record Key

f9243b58-5f7b-488e-851a-e8d99a5999fc

Public Version Date

June 23, 2021

Public Version Number

1

DI Record Publish Date

June 15, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"GEISTLICH PHARMA AG" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 45
U Unclassified 12