P.R.P MEMBRANE KIT

GUDID 08800041065714

Surgident Co.,Ltd.

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Primary Device ID	08800041065714
NIH Device Record Key	fc576936-ea79-477f-a442-88f665103984
Commercial Distribution Status	In Commercial Distribution
Brand Name	P.R.P MEMBRANE KIT
Version Model Number	ME-PRP
Company DUNS	689846448
Company Name	Surgident Co.,Ltd.
Device Count	1
DM Exempt	true
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	true
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	08800041065714 [Primary]

FDA Product Code

NDP	Accessories, Implant, Dental, Endosseous