HOSE,O2,DISS/SCHRADER 8 F 8038

GUDID 00816711023142

HOSE,O2,DISS/SCHRADER 8 F

PARKER-HANNIFIN CORPORATION

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• Primary Device ID: 00816711023142
• NIH Device Record Key: 4c625f2d-4695-4f93-9859-e28a009ee05a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HOSE,O2,DISS/SCHRADER 8 F
• Version Model Number: 8038
• Catalog Number: 8038
• 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	00816711023142 [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

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