MedLED Classic

GUDID 00812444029048

Portable Soft Strap Headlamp

RIVERPOINT MEDICAL, LLC

Head-worn lamp

• Primary Device ID: 00812444029048
• NIH Device Record Key: d6ca228b-0ff5-4dda-8755-e8ac218f4ef0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MedLED Classic
• Version Model Number: ML001-SK
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• 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: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812444029048 [Primary]

FDA Product Code

• HPP: Headlamp, Operating, Battery-Operated

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: 2024-04-26
• Device Publish Date: 2024-04-18

Devices Manufactured by RIVERPOINT MEDICAL, LLC

• 00840277411068 - HS Fiber: 2026-02-03 Suture
• 00840277411396 - HS Fiber: 2026-01-21 Blue/White UHMWPE Polyblend Braided Non-Absorbable Suture Tape
• 10840277411409 - HS Fiber: 2026-01-21 White/Blue UHMWPE polyblend braided non-absorbable suture.
• 00840277410023 - ProZip Knotless Implant: 2026-01-14 ProZip Knotless Implant
• 00840277410030 - ProZip Knotless Implant: 2026-01-14 ProZip Knotless Implant
• 10840277410068 - ProZip Knotless Implant: 2026-01-14 ProZip Knotless Implant
• 10840277410075 - ProZip Knotless Implant: 2026-01-14 ProZip Knotless Implant
• 00840277411365 - ApeLoop: 2025-12-17 Suture