Provi Bond, 5 ml - temporary cement, non eugenol - bisico Bielefelder Dentalsilicone GmbH & Co. KG

Duns Number:316133664

Device Description: temporary cement, non eugenol

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More Product Details

Catalog Number

03710

Brand Name

Provi Bond, 5 ml

Version/Model Number

03710

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

K973201

Product Code Details

Product Code

EMA

Product Code Name

Cement, Dental

Device Record Status

Public Device Record Key

da397963-a04d-4b28-b4d8-b69e6a01a126

Public Version Date

June 29, 2020

Public Version Number

4

DI Record Publish Date

January 18, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BISICO BIELEFELDER DENTALSILICONE 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 32
2 A medical device with a moderate to high risk that requires special controls. 74