5300010947

GUDID 07613153000761

10.0mm Tapered Dermabrader Medium

STRYKER CORPORATION

Dermatome blade, single-use
Primary Device ID07613153000761
NIH Device Record Key5bbd3484-d0b7-437c-bb7a-c2b6c96506a7
Commercial Distribution StatusIn Commercial Distribution
Version Model Number5300010947
Catalog Number5300010947
Company DUNS196548481
Company NameSTRYKER CORPORATION
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 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
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Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS107613153000761 [Primary]

FDA Product Code

GFEBRUSH, DERMABRASION, POWERED

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-24
Device Publish Date2018-09-23

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