DirectMed, Inc.

GUDID 00850038863166

Extension Set with 0.2um filter

Directmed, Inc.

Intravenous administration tubing extension set

• Primary Device ID: 00850038863166
• NIH Device Record Key: 921463d2-3816-4751-9599-b43348174c0b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DirectMed, Inc.
• Version Model Number: SM-007
• Company DUNS: 969484237
• Company Name: Directmed, Inc.
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850038863166 [Primary]

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: 2024-05-13
• Device Publish Date: 2024-05-03

On-Brand Devices [DirectMed, Inc. ]

• 10850038863118: EXTENSION SET 7" SMALLBORE
• 10850038863101: EXTENSION SET 7” SMALLBORE BONDED VALVE
• 00850038863111: EXTENSION SET 7" SMALLBORE
• 00850038863104: EXTENSION SET 7” SMALLBORE BONDED VALVE
• 10850038863163: Extension Set with 0.2um filter
• 00850038863166: Extension Set with 0.2um filter
• 10850038863170: Administration Set-Female Luer lock, 150µm Filter w/Male Luer Lock, Sterile
• 00850038863173: Administration Set-Female Luer lock, 150µm Filter w/Male Luer Lock, Sterile