Avanos 3520E

GUDID 00761887001817

PRYOR PRODUCTS

Intravenous pole

• Primary Device ID: 00761887001817
• NIH Device Record Key: b03f6f3d-1147-4854-bbe5-3fa8f1c8a3ab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Avanos
• Version Model Number: 3520E
• Catalog Number: 3520E
• Company DUNS: 073386039
• Company Name: PRYOR PRODUCTS
• Device Count: 1
• DM Exempt: true
• 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: false
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00761887001817 [Primary]

FDA Product Code

• FOX: Stand, Infusion

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: 2020-01-09
• Device Publish Date: 2020-01-01

On-Brand Devices [Avanos]

• 00761887001817: 3520E
• 00761887003903: Avanos Convers Kit/Cortak/Halyard
• 00761887003316: Clamp receiver unit cover