FOREFOOT 119006S

GUDID 10381780045151

Sterile drill for the introduction of the compression staples or screws.

NEWDEAL

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• Primary Device ID: 10381780045151
• NIH Device Record Key: 1e7cf40a-910e-46d8-911e-79f324ce018e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FOREFOOT
• Version Model Number: 119006SND
• Catalog Number: 119006S
• Company DUNS: 536935331
• Company Name: NEWDEAL
• 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: true
• 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(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com

Device Dimensions

• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter
• Length: 41 Millimeter
• Device Size Text, specify: 0
• Outer Diameter: 2.2 Millimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged
• Special Storage Condition, Specify: Between 0 and 0 *Do Not Use if Package is Damaged

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780045151 [Primary]

FDA Product Code

• HTW: BIT, DRILL

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-01-07
• Device Publish Date: 2020-12-30

On-Brand Devices [FOREFOOT]

• 10381780064398: The principal of the FOREFOOT sets is to propose a group of implants (screws and staples) and th
• 10381780045151: Sterile drill for the introduction of the compression staples or screws.
• 10381780045144: Non-sterile drill for the introduction of compression staples or screws.