ET RIGID RETRACTION CAP

GUDID 00810125991202

HIOSSEN, INC.

Dental implant suprastructure, temporary, preformed, single-use
Primary Device ID00810125991202
NIH Device Record Key04725356-159d-45dd-abc8-d3c5fbcf1588
Commercial Distribution StatusIn Commercial Distribution
Brand NameET RIGID RETRACTION CAP
Version Model NumberETRRC760C
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
GS100810125991202 [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 Date2024-07-11
Device Publish Date2024-07-03

On-Brand Devices [ET RIGID RETRACTION CAP]

00810019240348ETRRC760
00810019240331ETRRC670
00810019240324ETRRC660
00810019240317ETRRC640
00810019240300ETRRC570
00810019240294ETRRC560
00810019240287ETRRC540
00810019240270ETRRC471
00810019240263ETRRC461
00810019240256ETRRC441
00810019240249ETRRC470
00810019240232ETRRC460
00810019240225ETRRC440
00810125991097ETRRC460C
00810125991080ETRRC440C
00810125991202ETRRC760C
00810125991196ETRRC670C
00810125991189ETRRC660C
00810125991172ETRRC640C
00810125991165ETRRC570C
00810125991158ETRRC560C
00810125991141ETRRC540C
00810125991134ETRRC471C
00810125991127ETRRC461C
00810125991110ETRRC441C
00810125991103ETRRC470C

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