Reprocessed 4mm EndoScrub Sheath, 30 deg

GUDID B39019120101

SURETEK MEDICAL

Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter Paranasal sinus irrigation catheter
Primary Device IDB39019120101
NIH Device Record Keya78e18aa-5868-44ca-b4d0-21bb88fa89f1
Commercial Distribution StatusIn Commercial Distribution
Brand NameReprocessed 4mm EndoScrub Sheath, 30 deg
Version Model Number19-12010
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
HIBCCB39019120101 [Primary]

FDA Product Code

KAMCannula, Sinus

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-23
Device Publish Date2021-06-15

On-Brand Devices [Reprocessed 4mm EndoScrub Sheath, 30 deg]

B3901912010119-12010
B3901912101191210

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