AIM

GUDID 05099169331884

Vitalograph AIM

VITALOGRAPH (IRELAND) LIMITED

Aerosol inhalation monitor

• Primary Device ID: 05099169331884
• NIH Device Record Key: fa92b5a3-0fb7-409c-a903-7ed188bb8d4b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AIM
• Version Model Number: 4500
• Company DUNS: 219683489
• Company Name: VITALOGRAPH (IRELAND) LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05099169331884 [Package]; Contains: 15099169331881; Package: [1 Units]; In Commercial Distribution
GS1	15099169331881 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K893665

FDA Product Code

• BWF: SPIROMETER, THERAPEUTIC (INCENTIVE)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-12-28
• Device Publish Date: 2021-12-20

On-Brand Devices [AIM]

• 35099169457394: 45739
• 35099169457387: 45738
• 05099169457379: 45737
• 05099169457355: 45735
• 35099169457349: 45734
• 35099169457332: 45733
• 35099169457325: 45732
• 35099169457103: 45710
• 05099169331884: Vitalograph AIM