novo.lign P veneer - novo.lign P veneer posterior 4W3 lower A10 4 - bredent GmbH & Co. KG

Duns Number:341086190

Device Description: novo.lign P veneer posterior 4W3 lower A10 4 parts (44,45,46,47) 1 Assortment

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More Product Details

Catalog Number

VU4W3A10

Brand Name

novo.lign P veneer

Version/Model Number

VU4W3A10

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)

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

ELM

Product Code Name

Denture, plastic, teeth

Device Record Status

Public Device Record Key

0e19f84a-dba1-44ac-be57-0ffd0dcb2d88

Public Version Date

March 10, 2021

Public Version Number

3

DI Record Publish Date

September 21, 2016

Additional Identifiers

Package DI Number

EBREVU4W3A109

Quantity per Package

1

Contains DI Package

EBREVU4W3A100

Package Discontinue Date

September 21, 2016

Package Status

Not in Commercial Distribution

Package Type

dummy

"BREDENT GMBH & CO. KG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 38
2 A medical device with a moderate to high risk that requires special controls. 375