SURFIX®

GUDID M248529061ND1

This K-Wire of diameter 2.5 mm and of length 250 mm is used to guide the instrumentation and the screws.

NEWDEAL

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• Primary Device ID: M248529061ND1
• NIH Device Record Key: c949f249-6eb4-48bb-bc7c-8837729bdd7c
• Commercial Distribution Discontinuation: 2027-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SURFIX®
• Version Model Number: 529061ND
• 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: 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
• 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 Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780043256 [Primary]
HIBCC	M248529061ND1 [Secondary]

FDA Product Code

• FZX: Guide, surgical, instrument

Sterilization

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

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

[M248529061ND1]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-09-18
• Device Publish Date: 2017-06-06

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• M248219027ND1: The SURFIX® ALPHA drilling guide is used to guide the drills while preparing the holes for the
• M248SET101ND1: This lid is used to ensure closing of both trays numbers SET000ND and SET100ND.
• M248SET100ND1: This tray is used for transport and sterilization of the instruments that are specific to the os
• M248SET000ND1: This tray is used for transport and sterilization of the instruments that are not specific to th
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• M248286338ND1: Stainless steel Newdeal non sterile locking system fixation consists of screws and washers. This
• M248286336SND1: Stainless steel Newdeal sterile locking system fixation consists of screws and washers. This sys
• M248286336ND1: Stainless steel Newdeal non sterile locking system fixation consists of screws and washers. This
• M248529061ND1: This K-Wire of diameter 2.5 mm and of length 250 mm is used to guide the instrumentation and the