Latarjet 71935609

GUDID 00885556707951

HALF CANNULA OBTURATOR - LONG

Smith & Nephew, Inc.

Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 00885556707951
• NIH Device Record Key: f0b6d028-7bcc-4740-838a-ff034923e575
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Latarjet
• Version Model Number: 71935609
• Catalog Number: 71935609
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556707951 [Primary]

FDA Product Code

• NBH: Accessories, arthroscopic

Sterilization

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

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

[00885556707951]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-13
• Device Publish Date: 2019-03-05

On-Brand Devices [Latarjet]

• 00885556716267: DIA. 15MM CANNULA COVER
• 00885556716250: DIA. 15MM CANNULA TUBE
• 00885556716243: DIA. 15MM CANNULA TROCAR
• 00885556708057: ARTHROSCOPIC LATARJET/BONE BLOCK LID
• 00885556708040: ARTHROSCOPIC LATARJET/BONE BLOCK TRAY
• 00885556708026: CORACOID DRILLING OFFSETGUIDE 10MM
• 00885556708019: CORACOID DRILLING GUIDE
• 00885556708002: SUBSCAP SPREADER SLIDING BLOCK
• 00885556707999: SUBSCAPULARIS SPREADER
• 00885556707982: SINGLE POSTERIOR GLENOID DRILL GUIDE
• 00885556707975: TISSUE RETRACTOR - 45 DEGREE
• 00885556707968: TISSUE RETRACTOR - 90 DEGREE
• 00885556707951: HALF CANNULA OBTURATOR - LONG
• 00885556707944: HALF CANNULA - LONG
• 00885556707791: SUTURE TENSIONER
• 00885556646489: OFFSET MEASUREMENT TOOL
• 00885556646472: ANTERIOR GLENOID DRILL GUIDE - 8MM
• 00885556646465: ANTERIOR GLENOID DRILL GUIDE - 7MM
• 00885556646458: ANTERIOR GLENOID DRILL GUIDE - 6MM
• 00885556646441: ANTERIOR GLENOID DRILL GUIDE - 5MM
• 00885556646434: CORACOID DRILL GUIDE 10MM OFFSET BLOCK
• 00885556646427: 5MM CORACOID DRILL GUIDE
• 00885556634196: BONE GRASPER
• 00885556746554: 9MM CIRCLE ANTERIOR DRILL GUIDE
• 00885556746547: 8MM CIRCLE ANTERIOR DRILL GUIDE
• 00885556746530: 7MM CIRCLE ANTERIOR DRILL GUIDE
• 00885556746509: 6MM CIRCLE ANTERIOR DRILL GUIDE
• 00885556746493: 9MM FORKED ANTERIOR DRILL GUIDE
• 00885556746479: 8MM FORKED ANTERIOR DRILL GUIDE
• 00885556746448: 7MM FORKED ANTERIOR DRILL GUIDE
• 00885556746431: 6MM FORKED ANTERIOR DRILL GUIDE
• 00885556746424: ADJUSTABLE GLENOID GUIDE