MollRing Cutter Transection Device 4200-41

GUDID 00840663102709

MollRing Cutter Transection Device, 6mm

LEMAITRE VASCULAR, INC.

Intraluminal artery stripper, reusable

• Primary Device ID: 00840663102709
• NIH Device Record Key: 4d118512-2b58-4f67-92a6-ac9a6cdea0f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MollRing Cutter Transection Device
• Version Model Number: 4200-41
• Catalog Number: 4200-41
• Company DUNS: 184805166
• Company Name: LEMAITRE VASCULAR, INC.
• 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: 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com
• Phone: 781-221-2266
• Email: csus@lemaitre.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840663102709 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K950813

FDA Product Code

• DWX: Stripper, Artery, Intraluminal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-07-15

On-Brand Devices [MollRing Cutter Transection Device]

• 00840663102747: MollRing Cutter Transection Device, 10mm
• 00840663102730: MollRing Cutter Transection Device, 9mm
• 00840663102723: MollRing Cutter Transection Device, 8mm
• 00840663102716: MollRing Cutter Transection Device, 7mm
• 00840663102709: MollRing Cutter Transection Device, 6mm
• 00840663102693: MollRing Cutter Transection Device, 5mm