RETRACTOR RING 516-856L

GUDID 00192896080959

RETRACTOR RING SOLID LARGE ROUND RING

SONTEC INSTRUMENTS, INC.

Laparotomy ring
Primary Device ID00192896080959
NIH Device Record Keyf21bdd61-b937-49c3-a4c2-aeb46e06a633
Commercial Distribution StatusIn Commercial Distribution
Brand NameRETRACTOR RING
Version Model Number516-856L
Catalog Number516-856L
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

Lumen/Inner Diameter12.5 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896080959 [Primary]

FDA Product Code

HXPINSTRUMENT, BENDING OR CONTOURING

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896080959]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-22
Device Publish Date2018-09-20

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