ALGERBRUSH BURR 11-4610

GUDID 00192896012639

ALGERBRUSH II CORNEAL RUST RING REMOVER BURR

SONTEC INSTRUMENTS, INC.

Corneal bur, rust ring removal, reusable
Primary Device ID00192896012639
NIH Device Record Key1e68f58f-2e99-484c-afc1-ea945188bdda
Commercial Distribution StatusIn Commercial Distribution
Brand NameALGERBRUSH BURR
Version Model Number11-4610
Catalog Number11-4610
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896012639 [Primary]

FDA Product Code

HOGBurr, Corneal, Battery-Powered

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896012639]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-05-14
Device Publish Date2018-09-18

On-Brand Devices [ALGERBRUSH BURR]

00192896012714ALGERBRUSH II PTERYGIUM BURR MEDIUM WHEEL
00192896012691ALGERBRUSH II PTERYGIUMFINE BURR WHEEL
00192896012677ALGERBRUSH II PTERYGIUM BURR MEDIUM BALL TIP
00192896012653ALGERBRUSH II PTERYGIUM BURRFINE BALL TIP
00192896012639ALGERBRUSH II CORNEAL RUST RING REMOVER BURR

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