Anastoclip Atraumatic Forceps 4001-06

GUDID 00840663102419

Anastoclip Atraumatic Forceps, 18cm

LEMAITRE VASCULAR, INC.

Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps Clip forceps

• Primary Device ID: 00840663102419
• NIH Device Record Key: bf9871b4-db50-4916-8235-0ce901de4717
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Anastoclip Atraumatic Forceps
• Version Model Number: 4001-06
• Catalog Number: 4001-06
• Company DUNS: 184805166
• Company Name: LEMAITRE VASCULAR, INC.
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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	00840663102419 [Primary]

FDA Product Code

• HTD: Forceps

Sterilization

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

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

[00840663102419]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-06-30

On-Brand Devices [Anastoclip Atraumatic Forceps]

• 00840663107285: Anastoclip Atraumatic Forceps, 20cm
• 00840663102419: Anastoclip Atraumatic Forceps, 18cm
• 00840663109609: Anastoclip Atraumatic Forceps, 20cm