LeMaitre Embolectomy Catheter 1601-24

GUDID 00840663100439

2F 40 cm LeMaitre Embolectomy Catheter

LEMAITRE VASCULAR, INC.

Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter Thrombectomy balloon catheter

• Primary Device ID: 00840663100439
• NIH Device Record Key: 63831e92-33a3-443d-a2b9-d7be114d5f0f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LeMaitre Embolectomy Catheter
• Version Model Number: 1601-24
• Catalog Number: 1601-24
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx
• Phone: 781-221-2266
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840663100439 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K992368

FDA Product Code

• DXE: Catheter, Embolectomy

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: 2015-06-30

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