SmartPeg Type 117 100809

GUDID 09010522002476

ISQ Measurement Peg

Osstell AB

Dental implant stability measurement peg
Primary Device ID09010522002476
NIH Device Record Key3d9a229e-bf14-4461-886f-a7a1f6370e3d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSmartPeg Type 117
Version Model NumberSmartPeg Type 117
Catalog Number100809
Company DUNS633171269
Company NameOsstell AB
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 Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS109010522002476 [Package]
Contains: 09010522002483
Package: Box [5 Units]
In Commercial Distribution
GS109010522002483 [Primary]

FDA Product Code

EKXHandpiece, Direct Drive, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-23
Device Publish Date2024-05-15

Devices Manufactured by Osstell AB

09010522000731 - Osstell ISQ Probe2024-09-19 ISQ Measurement Instrument Accessory
09010522002315 - Osstell SmartPeg Type 1102024-09-19 ISQ Measurement Peg
09010522002322 - Osstell SmartPeg Type 1112024-09-19 ISQ Measurement Peg
09010522000847 - Osstell IDx Instrument2024-06-04 ISQ Measurement Instrument
09010522001134 - DIO IDx Instrument2024-06-04 ISQ Measurement Instrument
09010522002476 - SmartPeg Type 1172024-05-23ISQ Measurement Peg
09010522002476 - SmartPeg Type 1172024-05-23 ISQ Measurement Peg
09010522002070 - SmartPeg Type 98 - Neoss2024-05-22 ISQ Measurement Peg
09010522002469 - Neoss SmartPeg Mount2023-12-14 SmartPeg Mount

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