NobelReplace® - Guided Abutment NobelReplace® RP - Nobel Biocare AB

Duns Number:353939929

Device Description: Guided Abutment NobelReplace® RP

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


More Product Details

Catalog Number

32906

Brand Name

NobelReplace®

Version/Model Number

32906

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 01, 2021

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

DZE

Product Code Name

IMPLANT, ENDOSSEOUS, ROOT-FORM

Device Record Status

Public Device Record Key

6b0cd60b-5d07-4b63-88d5-18ca1c5f86ad

Public Version Date

May 20, 2022

Public Version Number

9

DI Record Publish Date

September 17, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"NOBEL BIOCARE AB" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 782
2 A medical device with a moderate to high risk that requires special controls. 3680