5300010943

GUDID 07613153000723

7.0mm Straight Dermabrader Medium

STRYKER CORPORATION

Dermatome blade, single-use
Primary Device ID07613153000723
NIH Device Record Key3b9dd5ed-06c3-4ac0-92f9-bbaf462ec1ac
Commercial Distribution StatusIn Commercial Distribution
Version Model Number5300010943
Catalog Number5300010943
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
GS107613153000723 [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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