Advanced Instruments Model 3250 Single-Sample Osmometer 3250

GUDID 00816068020870

The Advanced Instruments 3250 Single-Sample Osmometer is designed for routine osmolality measurement in pharma, biotech, and food and beverage labs. Providing accurate and precise osmolality measurement, with an operating range of 0-4000 mOsm.

ADVANCED INSTRUMENTS, INC.

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• Primary Device ID: 00816068020870
• NIH Device Record Key: ae18c54c-55b2-4cb9-bf79-351af744cc76
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Advanced Instruments Model 3250 Single-Sample Osmometer
• Version Model Number: 3250
• Catalog Number: 3250
• Company DUNS: 125006353
• Company Name: ADVANCED INSTRUMENTS, INC.
• 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: 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: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com
• Phone: +17813209000
• Email: Orders@aicompanies.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816068020870 [Primary]

FDA Product Code

• JJM: Osmometer For Clinical Use

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: 2020-09-29
• Device Publish Date: 2020-09-21

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