HMG IV Administration Set

GUDID 00850048235144

100” (254cm) Primary Administration Set With Universal Spike Drip Chamber with Needle Free Y-site

Hartman Medical Group LLC

Basic intravenous administration set, noninvasive

• Primary Device ID: 00850048235144
• NIH Device Record Key: 984e3894-e0c4-4161-92da-35bad9529900
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HMG IV Administration Set
• Version Model Number: FCA1002
• Company DUNS: 117654675
• Company Name: Hartman Medical Group LLC
• Device Count: 50
• 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: true
• 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	00850048235144 [Unit of Use]
GS1	10850048235141 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150513

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: 2025-04-28
• Device Publish Date: 2025-04-20

On-Brand Devices [HMG IV Administration Set]

• 00850048235144: 100” (254cm) Primary Administration Set With Universal Spike Drip Chamber with Needle Free Y-s
• 00850048235137: 100” (254cm) Primary Administration Set With Universal Spike Drip Chamber