DEMARRES RETRACTOR 10-4214

GUDID 00192896072305

DEMARRES RETRACTOR BLUE ELECTRO COATED

SONTEC INSTRUMENTS, INC.

Eyelid speculum, reusable
Primary Device ID00192896072305
NIH Device Record Keyf1fc445a-2381-48bd-b2e0-d3c26be8d54e
Commercial Distribution StatusIn Commercial Distribution
Brand NameDEMARRES RETRACTOR
Version Model Number10-4214
Catalog Number10-4214
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
GS100192896072305 [Primary]

FDA Product Code

HNIRetractor, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896072305]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-22
Device Publish Date2018-09-19

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