AIM

GUDID 05099169331884

Vitalograph AIM

VITALOGRAPH (IRELAND) LIMITED

Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor Aerosol inhalation monitor
Primary Device ID05099169331884
NIH Device Record Keyfa92b5a3-0fb7-409c-a903-7ed188bb8d4b
Commercial Distribution StatusIn Commercial Distribution
Brand NameAIM
Version Model Number4500
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

Device Identifiers

Device Issuing AgencyDevice ID
GS105099169331884 [Package]
Contains: 15099169331881
Package: [1 Units]
In Commercial Distribution
GS115099169331881 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BWFSPIROMETER, THERAPEUTIC (INCENTIVE)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-12-28
Device Publish Date2021-12-20

On-Brand Devices [AIM]

3509916945739445739
3509916945738745738
0509916945737945737
0509916945735545735
3509916945734945734
3509916945733245733
3509916945732545732
3509916945710345710
05099169331884Vitalograph AIM
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