MTD 4000 Digital Traction ME 4000

GUDID 00816864020197

Mettler Traction Decompression system, head unit

METTLER ELECTRONICS CORP.

Programmable powered traction system Programmable powered traction system Programmable powered traction system

• Primary Device ID: 00816864020197
• NIH Device Record Key: 2efe9e04-77de-40fc-9600-f69b6c211e27
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MTD 4000 Digital Traction
• Version Model Number: ME 4000
• Catalog Number: ME 4000
• Company DUNS: 008513913
• Company Name: METTLER ELECTRONICS CORP.
• 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(714)533-2221
• Email: service@mettlerelectronics.com
• Phone: +1(714)533-2221
• Email: service@mettlerelectronics.com
• Phone: +1(714)533-2221
• Email: service@mettlerelectronics.com

Device Dimensions

• Weight: 44 Pound
• Weight: 44 Pound
• Weight: 44 Pound

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *No
• Special Storage Condition, Specify: Between 0 and 0 *No

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816864020197 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K091540

FDA Product Code

• ITH: EQUIPMENT, TRACTION, POWERED

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: 2018-07-06
• Device Publish Date: 2016-09-15

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