Avanos 70208384

GUDID 00761887003903

Avanos Convers Kit/Cortak/Halyard

PRYOR PRODUCTS

Intravenous pole

• Primary Device ID: 00761887003903
• NIH Device Record Key: a1897ec1-0fcf-464a-adf0-535ef2356b02
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Avanos
• Version Model Number: 70208384
• Catalog Number: 70208384
• Company DUNS: 073386039
• Company Name: PRYOR PRODUCTS
• 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: 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	00761887003903 [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: 2022-03-25
• Device Publish Date: 2022-03-17

On-Brand Devices [Avanos]

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