HOSE ASSY,O2 DISS,OHMEDA 8072

GUDID 00816711023234

HOSE ASSY,O2 DISS,OHMEDA

PARKER-HANNIFIN CORPORATION

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• Primary Device ID: 00816711023234
• NIH Device Record Key: 2c7e0e91-2b6c-4742-bb59-69edf7616ba1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HOSE ASSY,O2 DISS,OHMEDA
• Version Model Number: 8072
• Catalog Number: 8072
• Company DUNS: 004175550
• Company Name: PARKER-HANNIFIN CORPORATION
• 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816711023234 [Primary]

FDA Product Code

• BYX: Tubing, Pressure And Accessories

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: 2022-12-12
• Device Publish Date: 2022-12-02

On-Brand Devices [HOSE ASSY,O2 DISS,OHMEDA]

• 00816711023388: HOSE ASSY,O2 DISS,OHMEDA
• 00816711023289: HOSE ASSY,O2 DISS,OHMEDA
• 00816711023272: HOSE ASSY,O2 DISS,OHMEDA
• 00816711023265: HOSE ASSY,O2 DISS,OHMEDA
• 00816711023258: HOSE ASSY,O2 DISS,OHMEDA
• 00816711023241: HOSE ASSY,O2 DISS,OHMEDA
• 00816711023234: HOSE ASSY,O2 DISS,OHMEDA