5450-815-107

GUDID 37613252518380

Sonic Control Serrated Knife

STRYKER CORPORATION

Soft-tissue ultrasonic surgical system handpiece tip, single-use
Primary Device ID37613252518380
NIH Device Record Key82965c46-6015-40a3-bc86-066e328bf1be
Commercial Distribution StatusIn Commercial Distribution
Version Model Number5450815107
Catalog Number5450-815-107
Company DUNS196548481
Company NameSTRYKER CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107613252518389 [Primary]
GS137613252518380 [Package]
Contains: 07613252518389
Package: pack [5 Units]
In Commercial Distribution

FDA Product Code

LFLInstrument, ultrasonic surgical

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-25
Device Publish Date2016-09-23

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