Soft/Fibra® 1/2 force

GUDID 10607915111530

Indicated for surgical clamping during cardiovascular peripheral vascular, and general surgery.

APPLIED MEDICAL RESOURCES CORPORATION

Vascular clamp, single-use Vascular clamp, single-use Vascular clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use Surgical bulldog clamp, single-use

• Primary Device ID: 10607915111530
• NIH Device Record Key: d2f5e59d-cd94-4f12-a680-3c792f93a62f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Soft/Fibra® 1/2 force
• Version Model Number: G-1252
• Company DUNS: 187129135
• Company Name: APPLIED MEDICAL RESOURCES CORPORATION
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com
• Phone: 1.949.713.8300
• Email: contact@appliedmedical.com

Device Dimensions

• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter
• Length: 12 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00607915111533 [Primary]
GS1	10607915111530 [Package]; Contains: 00607915111533; Package: [15 Units]; In Commercial Distribution

FDA Product Code

• DSS: Clip, Vascular

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: 2015-07-20

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• 10607915140813 - Voyant Maryland Fusion Device with Single-Step Activation: 2023-04-04 Electrosurgical Sealer and Divider handpiece
• 10607915145313 - GelPOINT V-Path: 2023-03-27 Transvaginal Access Platform with Insufflation Stabilization System
• 10607915145320 - GelPOINT V-Path: 2023-03-27 Transvaginal Access Platform with Insufflation Stabilization System