Spatula Double-Hole Cannula

GUDID 04260632790502

Möller Medical GmbH

Liposuction system cannula, single-use

• Primary Device ID: 04260632790502
• NIH Device Record Key: b76aee92-c683-4eb0-b94b-7c9accd3a827
• Commercial Distribution Discontinuation: 2025-12-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Spatula Double-Hole Cannula
• Version Model Number: ASC-S820-25-0150
• Company DUNS: 320405061
• Company Name: Möller Medical GmbH
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260632790502 [Primary]

FDA Product Code

• GEA: Cannula, Surgical, General & Plastic Surgery

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-12-03
• Device Publish Date: 2019-05-07

On-Brand Devices [Spatula Double-Hole Cannula]

• 04260277178291: ASC-S820-30-0150
• 04260632790144: ASC-R820-30-0150
• 04260632790120: ASC-R820-25-0150
• 04260632790502: ASC-S820-25-0150