PMGF090NY

GUDID 10850005864407

90" Flow regulator, pinch clamp, male spin luer lock

PATHEN MEDICAL LLC

Intravenous administration tubing extension set

• Primary Device ID: 10850005864407
• NIH Device Record Key: 7aad2030-d80e-4912-a4aa-5665d9b6f902
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PMGF090NY
• Version Model Number: PMGF090NY
• Company DUNS: 042928915
• Company Name: PATHEN MEDICAL LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8773185421
• Email: questions@pathen.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850005864400 [Primary]
GS1	10850005864407 [Package]; Contains: 00850005864400; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• FPA: Set, Administration, Intravascular

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-07-23
• Device Publish Date: 2019-07-15

On-Brand Devices [PMGF090NY]

• 10850005864414: 90" Flow regulator, 1 needle free Y site, 8" above distal tip, pinch clamp,.22 micron filter, ma
• 10850005864407: 90" Flow regulator, pinch clamp, male spin luer lock