n!ce for Planmill - n!ce® for PlanMill®, LT A3.5, C14 - Institut Straumann AG

Duns Number:483599259

Device Description: n!ce® for PlanMill®, LT A3.5, C14

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More Product Details

Catalog Number

010.7148

Brand Name

n!ce for Planmill

Version/Model Number

Milling Materials

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

MR Safe

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

K173410,K173410

Product Code Details

Product Code

EIH

Product Code Name

POWDER, PORCELAIN

Device Record Status

Public Device Record Key

bf31d333-adda-4b75-a234-8d259e96307c

Public Version Date

May 29, 2019

Public Version Number

1

DI Record Publish Date

May 21, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"INSTITUT STRAUMANN AG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 52
2 A medical device with a moderate to high risk that requires special controls. 2726
3 A medical device with high risk that requires premarket approval 5