Reprocessed Micro Oscillating Sagittal Blade, 18.5 x 7.0mm

GUDID B3902296331141

SURETEK MEDICAL

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Primary Device IDB3902296331141
NIH Device Record Key2e505618-6312-4353-b71c-d6b7eb208ccb
Commercial Distribution StatusIn Commercial Distribution
Brand NameReprocessed Micro Oscillating Sagittal Blade, 18.5 x 7.0mm
Version Model Number2296-33-114
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
HIBCCB3902296331141 [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

Devices Manufactured by SURETEK MEDICAL

B390229631251 - Reprocessed Long Medium Blade, 31 x 9mm2021-05-04
B390229632121 - Reprocessed Micro Oscillating Sagittal Blade,18 x 5.5 mm2021-05-04
B3902296331141 - Reprocessed Micro Oscillating Sagittal Blade, 18.5 x 7.0mm2021-05-04
B3902296331141 - Reprocessed Micro Oscillating Sagittal Blade, 18.5 x 7.0mm2021-05-04
B3902296332121 - Reprocessed Micro Oscillating Sagittal Blade,18 x 5.5 mm2021-05-04
B3902296332251 - Reprocessed Long Medium Aggressive Blade, 31 x 9mm2021-05-04
B390229634121 - Reprocessed Medium Narrow Blade, 18 x 5.5mm2021-05-04
B390229635041 - Reprocessed Oscillating Saw Blade, 34.5 x 16.5mm2021-05-04
B390229635111 - Reprocessed Aggressive Medium Blade, 25 x 9 mm2021-05-04

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