COX for BIO-FEATHER

GUDID 18055002903872

Introducer 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 ID18055002903872
NIH Device Record Key0db9d0f5-8b97-47fe-97fb-1a1af37b53aa
Commercial Distribution StatusIn Commercial Distribution
Brand NameCOX for BIO-FEATHER
Version Model NumberCB20100-00
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
GS108055002903875 [Primary]
GS118055002903872 [Package]
Contains: 08055002903875
Package: [10 Units]
In Commercial Distribution

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 Date2018-03-07

On-Brand Devices [COX for BIO-FEATHER]

18056772678809Introducer coaxial needle
18056515883927Coaxial introducer needle
18055002909287Introducer coaxial needle
18055002903896Introducer coaxial needle
18055002903872Introducer coaxial needle
18055002903865Introducer coaxial needle
18055002903841Introducer coaxial needle
18055002903810Introducer coaxial needle
18055002903803Introducer coaxial needle
18055002903773Introducer coaxial needle
18055002903759Coaxial introducer needle
18055002903735Introducer coaxial needle
18055002903698Introducer Coaxial needle
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