Delikit Bite Registration

GUDID 08800024203232

Silicone dental impression material

Primary Device ID	08800024203232
NIH Device Record Key	67560fc3-bc52-4272-a328-0d1aa5a3af0b
Commercial Distribution Status	In Commercial Distribution
Brand Name	Delikit Bite Registration
Version Model Number	Delikit Bite Registration (50ml * 10 Cartridges)
Company DUNS	557822311
Company Name	Sherpakorea
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	08800024203232 [Primary]

ELW	Material, Impression

Steralize Prior To Use	false
Device Is Sterile	false

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