FineEtch 101-1201

GUDID 08809262954036

Dental etching solution

Primary Device ID	08809262954036
NIH Device Record Key	7e991e25-4ea3-45a7-89c2-e539bb77777a
Commercial Distribution Status	In Commercial Distribution
Brand Name	FineEtch
Version Model Number	101-1201
Catalog Number	101-1201
Company DUNS	689370711
Company Name	Spident 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	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00194202309204 [Package] Package: [180 Units] Discontinued: 2023-09-20 In Commercial Distribution
GS1	00202202110178 [Package] Package: [200 Units] In Commercial Distribution
GS1	08809262954036 [Primary]
GS1	20200101161714 [Package] Package: [100 Units] Discontinued: 2019-05-16 Not in Commercial Distribution

NDP	Accessories, Implant, Dental, Endosseous

Steralize Prior To Use	false
Device Is Sterile	false

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