Delikit Bite Registration

GUDID 08800024201894

Sherpakorea

Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material Silicone dental impression material
Primary Device ID08800024201894
NIH Device Record Key2fee51a3-6e9a-473b-9f14-02110aceed8b
Commercial Distribution StatusIn Commercial Distribution
Brand NameDelikit Bite Registration
Version Model NumberDelikit Bite Registration (50ml * 4 Cartridges)
Company DUNS557822311
Company NameSherpakorea
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com
Phone+827078429961
Emailhappidenco@naver.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108800024201894 [Primary]

FDA Product Code

ELWMaterial, Impression

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-12
Device Publish Date2021-01-04

On-Brand Devices [Delikit Bite Registration]

08800024201573Delikit Bite Registration (50ml * 200 Cartridges)
08800024201535Delikit Bite Registration (50ml * 50 Cartridges)
08800024201894Delikit Bite Registration (50ml * 4 Cartridges)
08800024203232Delikit Bite Registration (50ml * 10 Cartridges)

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