VirtuEye V1 E 01 1420

GUDID EFIAE0114201

Accessory to Fiagon navigation systems. Device for registration.

Fiagon GmbH

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Primary Device IDEFIAE0114201
NIH Device Record Keyb204f9f1-a4fd-4d07-95d5-788ffd84b6a4
Commercial Distribution StatusIn Commercial Distribution
Brand NameVirtuEye V1
Version Model Number1
Catalog NumberE 01 1420
Company DUNS312623008
Company NameFiagon GmbH
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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
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
HIBCCEFIAE0114201 [Primary]

FDA Product Code

PGWEar, Nose, And Throat Stereotaxic Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-06-21
Device Publish Date2021-06-11

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