Reprocessed 2.0mm Cannulated Drill Bit, QC, 150mm

GUDID B3903102211

SURETEK MEDICAL

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Primary Device IDB3903102211
NIH Device Record Key9f258562-ebf3-4a6e-b5ff-78d2c55dd969
Commercial Distribution StatusIn Commercial Distribution
Brand NameReprocessed 2.0mm Cannulated Drill Bit, QC, 150mm
Version Model Number310.221
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
HIBCCB3903102211 [Primary]

FDA Product Code

HTWBit, Drill

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-04
Device Publish Date2021-04-26

On-Brand Devices [Reprocessed 2.0mm Cannulated Drill Bit, QC, 150mm]

B3093102211310.221
B3903102211310.221

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