debritom+

GUDID 07649996166036

debritom+ micro water jet device

Medaxis AG

Surgical/orthopaedic lavage control unit

• Primary Device ID: 07649996166036
• NIH Device Record Key: 15aa4e1f-0068-4463-85c6-60c5920e7bd8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: debritom+
• Version Model Number: 1000.0005
• Company DUNS: 480870674
• Company Name: Medaxis AG
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +41628238800
• Email: info@medaxis.ch
• Phone: +41628238800
• Email: info@medaxis.ch
• Phone: +41628238800
• Email: info@medaxis.ch
• Phone: +41628238800
• Email: info@medaxis.ch
• Phone: +41628238800
• Email: info@medaxis.ch
• Phone: +41628238800
• Email: info@medaxis.ch
• Phone: +41628238800
• Email: info@medaxis.ch
• Phone: +41628238800
• Email: info@medaxis.ch
• Phone: +41628238800
• Email: info@medaxis.ch

Device Identifiers

Device Issuing Agency	Device ID
GS1	07649996166036 [Primary]
HIBCC	B724100000050 [Previous]

FDA Product Code

• FQH: Lavage, Jet

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: 2021-09-20
• Device Publish Date: 2021-09-10

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• 07649996166036: debritom+ micro water jet device