IPP-ON®

GUDID M248239011ND1

The distal PIP Fusion hand drill is used to prepare the distal phalanx and to define the size of the implant. This model is size 1.

NEWDEAL

Manual surgical rotary handpiece, reusable

• Primary Device ID: M248239011ND1
• NIH Device Record Key: c28e6474-1916-4c23-8d4a-477bb22eaf16
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IPP-ON®
• Version Model Number: 239011ND
• 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: 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: 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780045007 [Primary]
HIBCC	M248239011ND1 [Secondary]

FDA Product Code

• HTO: REAMER

Sterilization

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

[M248239011ND1]

Moist Heat or Steam Sterilization

[M248239011ND1]

Moist Heat or Steam Sterilization

[M248239011ND1]

Moist Heat or Steam Sterilization

[M248239011ND1]

Moist Heat or Steam Sterilization

[M248239011ND1]

Moist Heat or Steam Sterilization

[M248239011ND1]

Moist Heat or Steam Sterilization

[M248239011ND1]

Moist Heat or Steam Sterilization

[M248239011ND1]

Moist Heat or Steam Sterilization

[M248239011ND1]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-09-20
• Device Publish Date: 2017-05-26

On-Brand Devices [IPP-ON®]

• M248239001ND1: The basis is part of the container which product number is 239000ND and that is used for transpo
• M248239000ND1: The container is used for transport and sterilization of instruments and non-sterile implants.
• M248239022ND1: The proximal PIP Fusion hand drill is used to prepare the proximal phalanx and to define the siz
• M248239021ND1: The distal PIP Fusion hand drill is used to prepare the distal phalanx and to define the size of
• M248239012ND1: The proximal PIP Fusion hand drill is used to prepare the proximal phalanx and to define the siz
• M248239011ND1: The distal PIP Fusion hand drill is used to prepare the distal phalanx and to define the size of
• M248239500ND1: The clamp holder is used to grip the implant.
• M248239030ND1: The PIP Fusion handle impactor is used to insert the implant in the distal part.