Reprocessed 4.0mm RADenoid Pediatric Blade, Curved

GUDID B39018840081

Reprocessed 4mm RADenoid Pediatric Blade, Curved

SURETEK MEDICAL

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Primary Device IDB39018840081
NIH Device Record Key5b1bae42-9480-4683-9dae-11caedcd53cb
Commercial Distribution StatusIn Commercial Distribution
Brand NameReprocessed 4.0mm RADenoid Pediatric Blade, Curved
Version Model Number18-84008
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
HIBCCB39018840081 [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 Date2021-06-22
Device Publish Date2021-06-14

On-Brand Devices [Reprocessed 4.0mm RADenoid Pediatric Blade, Curved]

B390840081Reprocessed 4mm RADenoid Pediatric Blade, Curved
B39018840081Reprocessed 4mm RADenoid Pediatric Blade, Curved

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