BUNGE EVISCERATION SPOON 12-4608

GUDID 00192896013599

BUNGE EVISCERATION SPOON STRAIGHT HEAD

SONTEC INSTRUMENTS, INC.

Lens spoon
Primary Device ID00192896013599
NIH Device Record Key93faa7bf-a1c4-49af-8284-38b81a9d7155
Commercial Distribution StatusIn Commercial Distribution
Brand NameBUNGE EVISCERATION SPOON
Version Model Number12-4608
Catalog Number12-4608
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

Outer Diameter11 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896013599 [Primary]

FDA Product Code

HNBSpoon, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896013599]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-09-26
Device Publish Date2018-09-18

On-Brand Devices [BUNGE EVISCERATION SPOON]

00192896013605BUNGE EVISCERATION SPOON STRAIGHT HEAD
00192896013599BUNGE EVISCERATION SPOON STRAIGHT HEAD
00192896013582BUNGE EVISCERATION SPOON STRAIGHT HEAD
00192896013575BUNGE EVISCERATION SPOON STRAIGHT HEAD
00192896013568BUNGE EVISCERATION SPOON STRAIGHT HEAD
00192896013551BUNGE EVISCERATION SPOON STRAIGHT HEAD

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