Guide Drill

GUDID 08800011262808

Point Nix Co., Ltd.

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Primary Device ID	08800011262808
NIH Device Record Key	32f476c4-a6dd-4afe-ba61-5a69572e6b3d
Commercial Distribution Status	In Commercial Distribution
Brand Name	Guide Drill
Version Model Number	OGD1900S
Company DUNS	695333960
Company Name	Point Nix Co., Ltd.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800011262808 [Primary]

FDA Product Code

DZA	Drill, Dental, Intraoral