GUDID 07640141626122

Belimed AG

Surgical utensil washer/disinfector

• Primary Device ID: 07640141626122
• NIH Device Record Key: 6ce6b98d-ea89-4598-a83d-6e6f90f0cd43
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: WD 750
• Company DUNS: 480030261
• Company Name: Belimed 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: 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

Customer Support Contacts

• Phone: 8432167424
• Email: sean.colwell@belimed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640141626122 [Primary]

FDA Product Code

• MEC: Disinfector, Medical Devices

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-03-19
• Device Publish Date: 2016-06-28

Devices Manufactured by Belimed AG

• 07640141626023 - NA: 2019-03-19
• 07640141626047 - NA: 2019-03-19
• 07640141626054 - NA: 2019-03-19
• 07640141626078 - NA: 2019-03-19
• 07640141626122 - NA: 2019-03-19
• 07640141626122 - NA: 2019-03-19
• 07640141626139 - NA: 2019-03-19
• 07640141626146 - NA: 2019-03-19
• 07640141626153 - NA: 2019-03-19