Spatula Single-Hole Cannula

GUDID 04260632792117

Möller Medical GmbH

Liposuction system cannula, single-use

• Primary Device ID: 04260632792117
• NIH Device Record Key: f9e5ea23-6251-44b8-90de-55a3072a9ce6
• Commercial Distribution Discontinuation: 2025-12-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Spatula Single-Hole Cannula
• Version Model Number: ASC-S810-30-0150
• 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	04260632792117 [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 Single-Hole Cannula]

• 04260277178284: ASC-S810-25-0150
• 04260632790052: ASC-R810-30-0150
• 04260632790045: ASC-R810-25-0150
• 04260632792117: ASC-S810-30-0150