ProV-Access Sterile Disposable Needle Guide 5400

GUDID 00841912105397

Pro-V Vascular Access Needle Guide Verification Kit

PROTEK MEDICAL PRODUCTS, INC.

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Primary Device ID00841912105397
NIH Device Record Key2bb355f8-0b80-47b1-943b-2258f4cadff3
Commercial Distribution StatusIn Commercial Distribution
Brand NameProV-Access Sterile Disposable Needle Guide
Version Model Number5400
Catalog Number5400
Company DUNS965417181
Company NamePROTEK MEDICAL PRODUCTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100841912105397 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ITXTransducer, Ultrasonic, Diagnostic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-10-07
Device Publish Date2018-02-09

On-Brand Devices [ProV-Access Sterile Disposable Needle Guide]

00841912105397Pro-V Vascular Access Needle Guide Verification Kit
108419121013895406
108419121013725405
108419121013655404
108419121013585403
108419121013415402
108419121013345401
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