PEAKOSIL - Product Name: Start KitThis product is a - NEOSIL Co., Ltd

Duns Number:690409169

Device Description: Product Name: Start KitThis product is a customized Start Kit that one content of the kit Product Name: Start KitThis product is a customized Start Kit that one content of the kit was replaced with the other product comparing to the ordinary Start Kit.It includes Light Body 1 EA, Heavy Body 1 EA, Putty 1 EA, Yellow Mix Tip 3 EA, Intra Oral Tip 3 EA & Green Mix Tip 3 EA instead of the contents of ordinary Start Kit(NSSK).

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More Product Details

Catalog Number

-

Brand Name

PEAKOSIL

Version/Model Number

NSSK-1

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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)

-

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

ELW

Product Code Name

Material, Impression

Device Record Status

Public Device Record Key

9fb7fcbd-3ae1-4176-93cc-78f34bb1ce33

Public Version Date

January 03, 2020

Public Version Number

6

DI Record Publish Date

September 21, 2017

Additional Identifiers

Package DI Number

18800026400063

Quantity per Package

25

Contains DI Package

08800026400066

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton

"NEOSIL CO., LTD" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 4