I-SIL Medium Body Regular Set 102-0301

GUDID 08809262959819

Vinyl Polysiloxane Impression material

Spident Co., Ltd.

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 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 Silicone dental impression material Silicone dental impression material Silicone dental impression material
Primary Device ID08809262959819
NIH Device Record Key1fe1cee4-edc9-4e79-b89d-2299a573684b
Commercial Distribution StatusIn Commercial Distribution
Brand NameI-SIL Medium Body Regular Set
Version Model Number102-0301
Catalog Number102-0301
Company DUNS689370711
Company NameSpident Co., Ltd.
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com
Phone201-944-0511
EmailSpident.usa@gmail.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100002022092209 [Package]
Package: [300 Units]
Discontinued: 2022-09-22
In Commercial Distribution
GS102020030918043 [Package]
Package: [350 Units]
Discontinued: 2019-09-30
Not in Commercial Distribution
GS102021022719020 [Package]
Package: [100 Units]
In Commercial Distribution
GS108809262959819 [Primary]

FDA Product Code

ELWMaterial, Impression

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2019-09-30
Device Publish Date2017-02-20

Devices Manufactured by Spident Co., Ltd.

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08809262954524 - Base It2021-01-26 Light-cured base/liner containing calcium hydroxyapatite in urethane methacrylate oligomer.
20200623170027 - EsFlow LV A2 Syringe2021-01-26
20200723170026 - EsFlow LV A3 Syringe2021-01-26
00210205180012 - EsCom100 A4 Syringe2021-01-26 Nano-hybrid universal composite resin for posterior and anterior restorations.
20210205180023 - EsCom 100 B1 Syringe2021-01-26
08809262955576 - EsCom 100 A1 Capsules2021-01-26
20200523170066 - EsCom 100 A3.5 Capsules2021-01-26
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