PRO3DURE GR-17 temporary - pro3dure medical GmbH

Duns Number:312947842

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More Product Details

Catalog Number

-

Brand Name

PRO3DURE GR-17 temporary

Version/Model Number

1kg - A2

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

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

K201827

Product Code Details

Product Code

EBG

Product Code Name

Crown And Bridge, Temporary, Resin

Device Record Status

Public Device Record Key

a2d7f657-08ac-49e5-b313-af514639ff8b

Public Version Date

October 29, 2021

Public Version Number

2

DI Record Publish Date

November 18, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"PRO3DURE MEDICAL GMBH" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 195
2 A medical device with a moderate to high risk that requires special controls. 35
U Unclassified 13