Trauma - Misc E0017070-1

GUDID 00885556791325

MODIFIED BLOCKING SCREW GUIDE

Smith & Nephew, Inc.

General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit

• Primary Device ID: 00885556791325
• NIH Device Record Key: 24c3260b-44b4-45f9-ab6f-8e7d10474f1c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trauma - Misc
• Version Model Number: E0017070-1
• Catalog Number: E0017070-1
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556791325 [Primary]

FDA Product Code

• FZX: Guide, surgical, instrument

Sterilization

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

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

[00885556791325]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-08-04
• Device Publish Date: 2020-07-27

On-Brand Devices [Trauma - Misc]

• 00885556739297: 205MM FORCEPS W/ BALL TIP
• 00885556739181: MODIFIED BLOCKING SCREW GUIDE
• 00885556726303: CANNULATED DEPTH GAUGE
• 00885556724835: 1.9MM X 300MM NON-THREADED GUIDE PIN
• 00885556721049: 1.9MM X 450MM GUIDE PIN
• 00885556719077: 3.2MM X 343MM SMOOTH ENDED DRILL TIP PIN
• 00885556719053: 1.9MM X 300MM NON-THREADED GUIDE PIN
• 00885556717585: CANNULATED DEPTH GAUGE
• 00885556717578: 3.2MM X 450MM DRILL TIP GUIDE PIN
• 00885556717561: CANNULATED DEPTH GAUGE
• 00885556717554: 3.2MM X 450MM DRILL TIP GUIDE PIN
• 00885556717455: MODIFIED BLOCKING SCREW GUIDE
• 00885556714249: MODIFIED 3.2MM PARALLEL PIN GUIDE
• 00885556709320: CANNULATED DEPTH GAUGE
• 00885556705636: 3.2MM X 450MM DRILL TIP GUIDE PINS
• 00885556705629: CANNULATED DEPTH GAUGE
• 00885556705612: 3.2MM X 450MM DRILL TIP GUIDE PINS
• 00885556705605: CANNULATED DEPTH GAUGE
• 00885556705537: 2.5MM HEX DRIVER WITH LARGE HANDLE
• 00885556744963: 3.4MM HEX DRIVER W/ HANDLE
• 00885556744956: 2.7MM HEX DRIVER W/ HANDLE
• 00885556748558: MODIFIED 6.5MM CANNULATED SCREW DRIVER
• 00885556774656: 205MM FORCEPS W/ BALL TIP
• 00885556789711: LARGE BENDING PRESS LOWER ANVIL
• 00885556789704: LARGE BENDING PRESS UPPER ANVIL
• 00885556791325: MODIFIED BLOCKING SCREW GUIDE
• 00885556794630: MODIFIED 6.5MM CANNULATED SCREW DRIVER
• 00885556871331: 2.5MM TARGETER DRILL BIT
• 00885556799291: EXTENDED T8 DRIVER SHAFT
• 00885556799284: EXTENDED T7 DRIVER SHAFT
• 00885556799277: EXTENDED T6 DRIVER SHAFT