HARTMAN EAR SPECULA 465-225-5

GUDID 00192896079588

HARTMAN EAR SPECULA

SONTEC INSTRUMENTS, INC.

Ear speculum, reusable
Primary Device ID00192896079588
NIH Device Record Keyb866354e-48a5-49cb-8d0f-97e8c2984d66
Commercial Distribution StatusIn Commercial Distribution
Brand NameHARTMAN EAR SPECULA
Version Model Number465-225-5
Catalog Number465-225-5
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 Diameter5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896079588 [Primary]

FDA Product Code

HNCSpecula, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896079588]

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 Date2018-09-20

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