PEAKOSIL

Basic Information

• Brand Name: PEAKOSIL
• Primary DI: 08800026400011
• Version / Model: NS033C
• Company Name: NEOSIL Co., Ltd
• Labeler DUNS: 690409169
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2017-09-21
• Public Version: 5
• Public Version Date: 2021-06-30
• Public Version Status: Update
• Public Device Record Key: dd5541ce-ba34-4b25-9fe6-ec329334ec7e

Device Description

Product Name:PEAKOSIL Light Body Regular Set

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
ELW	Material, Impression	Dental	872.3660	2

GMDN Terms

Code	Name	Definition	Implantable	Status
35866	Silicone dental impression material	An elastomeric, polysiloxane-based material capable of reacting to form a rubber-like substance suitable to reproduce the structure of a patient's teeth and gums, or other oral anatomy, after being placed on an impression tray and inserted into the mouth. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	18800026400018	GS1		4	In Commercial Distribution
Primary	08800026400011	GS1
Package	08800026400332	GS1	Box	4	In Commercial Distribution

Premarket Submissions

Submission Number	Supplement Number
K152180	000