COX for MEDONE

GUDID 08053329376167

Inroducer coaxial needle

MEDAX SRL UNIPERSONALE

Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Nonimplantable needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use Needle guide, single-use
Primary Device ID08053329376167
NIH Device Record Key9f079b33-6fea-434e-a964-09cff867c24c
Commercial Distribution StatusIn Commercial Distribution
Brand NameCOX for MEDONE
Version Model NumberCO14100-00
Company DUNS440211428
Company NameMEDAX SRL UNIPERSONALE
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108053329376167 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KNWInstrument, Biopsy

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-10-07
Device Publish Date2018-03-06

On-Brand Devices [COX for MEDONE]

18053329376430Introducer Coaxial needle
18053329376416Introducer Coaxial Needle
18053329376393Introducer Coaxial needle
18053329376355Introducer Coaxial Needle
18053329376331Introducer Coaxial needle
18053329376287Introducer Coaxial needle
08053329376266Introducer Coaxial needle
18053329376249Inroducer Coaxial needle
18053329376188Introducer Coaxial needle
08053329376167Inroducer coaxial needle
08053329376105Coaxial Introducer needle
08053329376082Coaxial introducer needle
18052283955675Introducer coaxial needle
18052283955668Introducer coaxial needle
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.