Kyphon Bone Biopsy Device

GUDID 00763000026851

BONE BIOPSY DEVICE F05A SIZE 3-RB

MEDTRONIC SOFAMOR DANEK, INC.

Bone access cannula
Primary Device ID00763000026851
NIH Device Record Key803486ae-7da3-4dfc-8d41-34600716de69
Commercial Distribution StatusIn Commercial Distribution
Brand NameKyphon Bone Biopsy Device
Version Model NumberF05A
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000026851 [Primary]

FDA Product Code

KIHDISPENSER, CEMENT

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-11-28
Device Publish Date2018-10-28

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