ET RIGID PROTECT CAP

GUDID 00810019240195

HIOSSEN, INC.

Dental implant suprastructure, temporary, preformed, single-use
Primary Device ID00810019240195
NIH Device Record Key2daa8b5a-8309-4cef-9f3c-ea55d03f98a7
Commercial Distribution StatusIn Commercial Distribution
Brand NameET RIGID PROTECT CAP
Version Model NumberETRPC6005S
Company DUNS796083090
Company NameHIOSSEN, INC.
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 Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810019240195 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-05-23
Device Publish Date2019-05-15

On-Brand Devices [ET RIGID PROTECT CAP]

00810019240218ETRPC7005S
00810019240201ETRPC6007S
00810019240195ETRPC6005S
00810019240188ETRPC6004S
00810019240171ETRPC5007S
00810019240164ETRPC5005S
00810019240157ETRPC5004S
00810019240140ETRPC4507
00810019240133ETRPC4505
00810019240126ETRPC4504
00810019240119ETRPC4007
00810019240102ETRPC4005
00810019240096ETRPC4004

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.