HEMORRHOIDAL LIGATOR

GUDID B0995085610

SIMPLE STYLE HEMORRHOIDAL LIGATOR WITH LOADING CONE

SONTEC INSTRUMENTS, INC.

Haemorrhoid ligator
Primary Device IDB0995085610
NIH Device Record Key5f2a024f-cc17-4f4a-a339-f1f13580589e
Commercial Distribution StatusIn Commercial Distribution
Brand NameHEMORRHOIDAL LIGATOR
Version Model Number508-561
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896044777 [Primary]
HIBCCB0995085610 [Previous]

FDA Product Code

FHNLigator, Hemorrhoidal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B0995085610]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0995085610]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B0995085610]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-08
Device Publish Date2018-09-06

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