Reprocessed Twist-in Cannula w/Obturator, 8.25mm x 7cm

GUDID B390AR65301

SURETEK MEDICAL

Bone access cannula
Primary Device IDB390AR65301
NIH Device Record Keya2b5959d-4f3f-4ff7-9519-8c208f578b71
Commercial Distribution StatusIn Commercial Distribution
Brand NameReprocessed Twist-in Cannula w/Obturator, 8.25mm x 7cm
Version Model NumberAR-6530
Company DUNS785616934
Company NameSURETEK MEDICAL
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

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB390AR65301 [Primary]

FDA Product Code

NBHAccessories, Arthroscopic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-10-28
Device Publish Date2024-10-18

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