ULTRASOFT™ 3202-1

GUDID 10650551068508

SURGICAL LUMEN TUBING

PMT CORPORATION

Suction system catheter, general-purpose

• Primary Device ID: 10650551068508
• NIH Device Record Key: 5267fbc4-4a22-4119-a2a9-65e6abf9c030
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ULTRASOFT™
• Version Model Number: 3202-1
• Catalog Number: 3202-1
• Company DUNS: 039576871
• Company Name: PMT CORPORATION
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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: 800-626-5463
• Email: info@pmtcorp.com
• Phone: 800-626-5463
• Email: info@pmtcorp.com

Device Dimensions

• Length: 6 Feet
• Length: 6 Feet
• Length: 6 Feet
• Length: 6 Feet
• Length: 6 Feet
• Length: 6 Feet

Device Identifiers

Device Issuing Agency	Device ID
GS1	00650551068501 [Primary]
GS1	10650551068508 [Package]; Contains: 00650551068501; Package: BOX [12 Units]; In Commercial Distribution

FDA Product Code

• KGZ: Accessories, Catheter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-11-15

On-Brand Devices [ULTRASOFT™]

• 10650551068508: SURGICAL LUMEN TUBING
• 10650551068492: SURGICAL LUMEN TUBING