AIM

Primary DI
05099169457355
Brand
AIM
Company
VITALOGRAPH (IRELAND) LIMITED
Model
4500
Device description
45735
Published
2017-02-20
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
BWFSPIROMETER, THERAPEUTIC (INCENTIVE)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
BWFSpirometer, Therapeutic (Incentive)Anesthesiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K893665000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K893665000AEROSOL INHALATION MONITORVitalograph , Ltd.1989-08-21BWF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
05099169457355PackageGS11In Commercial Distribution
35099169457356PackageGS125In Commercial Distribution
15099169457352PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
05099169457355050991694573555099169457355
3509916945735635099169457356
1509916945735215099169457352

GMDN Terms#

Term, Definition table
TermDefinition
Aerosol inhalation monitorAn electronic device intended to be used in the assessment and training of a patient's inhalation flow rates and "firing" coordination when using an aerosol metered dose inhaler (MDI) or a dry powder inhaler (DPI). It is typically known as an aerosol inhalation monitor (AIM), and includes a display/control panel, an electronic flowmeter, a placebo MDI aerosol canister, and a flowhead with mouthpiece. The patient demonstrates his/her inhalation technique while the healthcare provider observes their performance; a visual incentive training device to encourage and motivate the patient, especially children, may be included.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Humidity10 Percent (%) Relative Humidity95 Percent (%) Relative Humidity
Storage Environment Temperature0 Degrees Celsius50 Degrees Celsius

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
219683489
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
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15099169283821PFT28202016-12-01
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05099169770508Pneumotrac68002017-11-15
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15099169331898Mouthpiece20202024-04-08
15099169203928Mouthpiece20202018-05-15
15099169251004Aspirator25102018-05-09
65099169688003SPIROTRAC70002021-04-30
15099169202013Mouthpiece20202016-12-08
15099169202020Mouthpiece20202018-05-15
15099169202426Safe-T-Way20242016-12-08
15099169202464Safe-T-Way20242016-12-08
15099169209203Safe-T-Way20242016-12-08
15099169209227Safe-T-Way20242016-12-08
15099169209241Safe-T-Way20242016-12-08
15099169209296Safe-T-Way20242018-05-15

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