Tumescence Infiltration Cannula

GUDID 04260632790564

Möller Medical GmbH

Liposuction system cannula, single-use

• Primary Device ID: 04260632790564
• NIH Device Record Key: 6d48d98e-78a4-4f75-9501-eeddedc06cae
• Commercial Distribution Discontinuation: 2025-12-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Tumescence Infiltration Cannula
• Version Model Number: ASC-S910-20-0150
• 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	04260632790564 [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 [Tumescence Infiltration Cannula]

• 04260277178376: ASC-S910-25-0150
• 04260277178369: ASC-S910-20-0250
• 04260277178352: ASC-S910-30-0350
• 04260277178345: ASC-S910-30-0250
• 04260632790618: ASC-R910-30-0350
• 04260632790601: ASC-R910-30-0250
• 04260632790588: ASC-R910-25-0250
• 04260632790571: ASC-R910-25-0150
• 04260632790540: ASC-R910-20-0250
• 04260632790533: ASC-R910-20-0150
• 04260632790595: ASC-S910-25-0250
• 04260632790564: ASC-S910-20-0150