Velox Pro

GUDID 08055002900478

MEDAX SRL UNIPERSONALE

Nonimplantable needle guide, single-use
Primary Device ID08055002900478
NIH Device Record Key096c7560-85f3-4b69-baf9-b29c25d803d8
Commercial Distribution StatusIn Commercial Distribution
Brand NameVelox Pro
Version Model NumberVP20100-00
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 Datefalse
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
GS108055002900478 [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 Number5
Public Version Date2019-10-07
Device Publish Date2016-09-21

On-Brand Devices [Velox Pro]

18056515887789VP18250-C0
18055002900994VP21160-C0
18055002900987VP21100-C0
18055002900970VP21160-00
18055002900949VP21100-00
18055002900529VP20200-C0
18055002900512VP20200-00
18055002900505VP20160-C0
18055002900499VP20160-00
18055002900482VP20100-C0
08055002900478VP20100-00
18055002900468VP20060-00
18055002900451VP18200-C0
18055002900444VP18200-00
18055002900437VP18160-C0
18055002900420VP18160-00
18055002900413VP18100-C0
18055002900406VP18100-00
18055002900390VP18060-00
18055002900383VP16200-C0
18055002900376VP16200-00
18055002900369VP16160-C0
18055002900352VP16160-00
18055002900345VP16100-C0
18055002900338VP16100-00
18055002900321VP14200-C0
18055002900314VP14200-00
18055002900307VP14160-C0
18055002900291VP14160-00
08055002900287VP14100-C0
18055002900277VP14100-00
18055002900260VP14060-00

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