SONTEC AORTIC PUNCH 2700-195

GUDID 00192896088320

SONTEC AORTIC PUNCH

SONTEC INSTRUMENTS, INC.

Aorta punch, reusable
Primary Device ID00192896088320
NIH Device Record Key177329a0-4327-453c-bc52-0bfa2648873e
Commercial Distribution StatusIn Commercial Distribution
Brand NameSONTEC AORTIC PUNCH
Version Model Number2700-195
Catalog Number2700-195
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 Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896088320 [Primary]

FDA Product Code

LRYPUNCH, SURGICAL

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896088320]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-12
Device Publish Date2018-09-11

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