71177135

GUDID 03596010601537

5.5MM CANNULATED DRILL BIT

Smith & Nephew, Inc.

Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use, sterile Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use Cannulated surgical drill bit, single-use

• Primary Device ID: 03596010601537
• NIH Device Record Key: 4eff9fa8-293b-495e-afb2-5d92c666bd3a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 71177135
• Catalog Number: 71177135
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• 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: 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: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	03596010601537 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123055

FDA Product Code

• HRS: PLATE, FIXATION, BONE

Sterilization

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

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

[03596010601537]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2020-10-22
• Device Publish Date: 2015-09-28

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• 00885556747407 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 1 RIGHT
• 00885556747414 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 2 RIGHT
• 00885556747421 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 3 RIGHT
• 00885556747438 - FASTPAK: 2024-06-21 FASTPAK TIBIAL BASE TRIAL SIZE 4 RIGHT