Reprocessed Micro Oscillating Sagittal Blade,18 x 5.5 mm

GUDID B390229632121

SURETEK MEDICAL

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Primary Device IDB390229632121
NIH Device Record Keyf7609f38-51e0-491a-be4d-b556260fd5c9
Commercial Distribution StatusIn Commercial Distribution
Brand NameReprocessed Micro Oscillating Sagittal Blade,18 x 5.5 mm
Version Model Number2296-3-212
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
HIBCCB390229632121 [Primary]

FDA Product Code

GFABlade, Saw, General & Plastic Surgery, Surgical

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 Micro Oscillating Sagittal Blade,18 x 5.5 mm]

B39022963321212296-33-212
B3902296321212296-3-212

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