Sarmix®M2000,100-240V no rotor 90.180.600

GUDID 04038917101974

Sarstedt Aktiengesellschaft & Co.KG

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• Primary Device ID: 04038917101974
• NIH Device Record Key: 44cce379-86aa-4601-9e71-4ab5b63f7ac8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sarmix®M2000,100-240V no rotor
• Version Model Number: 90.180.600
• Catalog Number: 90.180.600
• Company DUNS: 388000270
• Company Name: Sarstedt Aktiengesellschaft & Co.KG
• Device Count: 1
• DM Exempt: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com
• Phone: +1(800)257-5101
• Email: customerservice.us@sarstedt.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04038917101974 [Primary]

FDA Product Code

• GLE: MIXER, BLOOD TUBE

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: 2022-12-08
• Device Publish Date: 2022-11-30

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