Optichamber Diamond 166401

GUDID 00817081026597

Valved Holding Chamber, Optichamber Diamond

A-M SYSTEMS, LLC

Medicine chamber spacer, reusable

• Primary Device ID: 00817081026597
• NIH Device Record Key: 18ae3d01-8e03-4bde-ba0e-9713c793e076
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Optichamber Diamond
• Version Model Number: Optichamber Diamond - 166401
• Catalog Number: 166401
• Company DUNS: 020275145
• Company Name: A-M SYSTEMS, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Serial Number: false
• 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: true

Customer Support Contacts

• Phone: 3606838300
• Email: sales@a-msystems.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817081026597 [Primary]

FDA Product Code

• NVP: Holding Chambers, Direct Patient Interface

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: 2020-04-21
• Device Publish Date: 2020-04-13

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