PMG0083

GUDID 10850005864490

83” 15 drop, non-vented drip chamber, roller clamp, pre-slit Y-site, needleless Y-site connector, ROTATING MALE LUER

PATHEN MEDICAL LLC

Intravenous administration tubing extension set

• Primary Device ID: 10850005864490
• NIH Device Record Key: cc51947a-f230-4fec-90b7-4dbd8ec5e2f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PMG0083
• Version Model Number: PMG0083
• 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	00850005864493 [Primary]
GS1	10850005864490 [Package]; Contains: 00850005864493; 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 [PMG0083]

• 10850005864506: 84” 10 drop, vented/non-vented drip chamber, roller clamp, pre-slit Y-site, needleless Y-site
• 10850005864490: 83” 15 drop, non-vented drip chamber, roller clamp, pre-slit Y-site, needleless Y-site connect