Mopec 0810-MPC-000

GUDID 00850020091003

The CMM 115V Autopsy Saw is an FDA Class I product used for performing autopsies, featuring a high-speed oscillating blade to cut through cadaver bone without harming soft tissue.

Contract Medical Manufacturing, Limited Liability Company

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• Primary Device ID: 00850020091003
• NIH Device Record Key: 11a59b01-1c2b-4add-9fb7-50e88f5bc764
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mopec
• Version Model Number: 115V Autopsy Saw
• Catalog Number: 0810-MPC-000
• Company DUNS: 868719191
• Company Name: Contract Medical Manufacturing, Limited Liability Company
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com
• Phone: 8003628491
• Email: customerservice@mopec.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850020091003 [Primary]

FDA Product Code

• HAB: Saw, Powered, And Accessories

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: 2023-06-15
• Device Publish Date: 2023-06-07