RS-Standard Internal Hex Plastic Surgical Kit-Prem

GUDID 07290105156310

ADIN DENTAL IMPLANT SYSTEMS LTD

Dental implant/prosthesis surgical procedure kit
Primary Device ID07290105156310
NIH Device Record Key2447f429-135d-4df3-9021-a40e9d3a4fda
Commercial Distribution StatusIn Commercial Distribution
Brand NameRS-Standard Internal Hex Plastic Surgical Kit-Prem
Version Model NumberRS6301
Company DUNS533289435
Company NameADIN DENTAL IMPLANT SYSTEMS LTD
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107290105156310 [Primary]

FDA Product Code

OFYDental Implant Surgical Tray

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07290105156310]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-04-23

On-Brand Devices [RS-Standard Internal Hex Plastic Surgical Kit-Prem]

07290105156327RS6301IN
07290105156310RS6301

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