Clariflo

GUDID 16971919460739

Ningbo Albert Novosino Co.,Ltd.

Intravenous pressure infusor, manual, reusable

• Primary Device ID: 16971919460739
• NIH Device Record Key: 77e16abc-bb86-4347-a257-166c84d71885
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Clariflo
• Version Model Number: RU3000PGS
• Company DUNS: 543014978
• Company Name: Ningbo Albert Novosino Co.,Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971919460732 [Primary]
GS1	16971919460739 [Package]; Contains: 06971919460732; Package: [5 Units]; In Commercial Distribution
GS1	26971919460736 [Package]; Package: [2 Units]; In Commercial Distribution

FDA Product Code

• KZD: Infusor, Pressure, For I.V. Bags

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: 2023-04-28
• Device Publish Date: 2023-04-20

On-Brand Devices [Clariflo]

• 16971919460739: RU3000PGS
• 16971919460722: RU1000PGS
• 16971919460296: 3000PGS
• 06971919460275: 500PGS