VitaloJAK

GUDID 05099169710023

Base VitaloJAK UK(1)

VITALOGRAPH (IRELAND) LIMITED

Cough ambulatory recording system Cough ambulatory recording system
Primary Device ID05099169710023
NIH Device Record Keycf23014f-9d37-46f5-bb58-7335b6dcef85
Commercial Distribution StatusIn Commercial Distribution
Brand NameVitaloJAK
Version Model Number7100
Company DUNS219683489
Company NameVITALOGRAPH (IRELAND) LIMITED
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Operating and Storage Conditions

Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity
Storage Environment HumidityBetween 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Identifiers

Device Issuing AgencyDevice ID
GS105099169710023 [Package]
Contains: 15099169710020
Package: [1 Units]
In Commercial Distribution
GS115099169710020 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DSHRECORDER, MAGNETIC TAPE, MEDICAL

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-11-08
Device Publish Date2018-05-14

On-Brand Devices [VitaloJAK]

05099169715103Base VITALOJAK INTERNATIONAL WEST(1)
05099169710238Base VITALOJAK - SHORT CABLE(1)
05099169710023Base VitaloJAK UK(1)
05099169715110Base VITALOJAK

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