DRYSDALE NUCLEUS MANIPULATOR T12-5850

GUDID 00192896013841

DRYSDALE NUCLEUS MANIPULATOR SPUD SHAPED ANGLED TIP TITANIUM

SONTEC INSTRUMENTS, INC.

Eye spud
Primary Device ID00192896013841
NIH Device Record Keyadf99857-3a81-49f8-b137-5437600a1d7c
Commercial Distribution StatusIn Commercial Distribution
Brand NameDRYSDALE NUCLEUS MANIPULATOR
Version Model NumberT12-5850
Catalog NumberT12-5850
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 Identifiers

Device Issuing AgencyDevice ID
GS100192896013841 [Primary]

FDA Product Code

HNASpud, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896013841]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-09-25
Device Publish Date2018-09-18

On-Brand Devices [DRYSDALE NUCLEUS MANIPULATOR]

00192896013841DRYSDALE NUCLEUS MANIPULATOR SPUD SHAPED ANGLED TIP TITANIUM
00192896013766DRYSDALE NECLEUS MANIPULATOR WITH ANTERIOR CAPSULE POLISHER SPUD SHAPED ANGLED TIP STAINLESS STE
00192896013759DRYSDALE NUCLEUS MANIPULATOR SPUD SHAPED ANGLED TIP STAINLESS STEEL

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