Trauma - Shoulders E0018145-6

GUDID 00885556912713

GLENOID REAMER HANDLE

Smith & Nephew, Inc.

Surgical instrument handle, non-torque-limiting

• Primary Device ID: 00885556912713
• NIH Device Record Key: f777a8f4-5f5b-4df7-a13a-4cc4992640ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trauma - Shoulders
• Version Model Number: E0018145-6
• Catalog Number: E0018145-6
• Company DUNS: 045483575
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556912713 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

[00885556912713]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-28
• Device Publish Date: 2023-09-20

On-Brand Devices [Trauma - Shoulders]

• 00885556807859: SHOULDER ASSEMBLY IMPACTION STAND
• 00885556871324: SHOULDER ASSEMBLY IMPACTION STAND
• 00885556912737: BASEPLATE INSERTER
• 00885556912720: RATCHET HANDLE
• 00885556912713: GLENOID REAMER HANDLE
• 00885556912706: 2.8MM DRILL SHAFT
• 00885556912690: HUMERAL REAMER SZ 4
• 00885556912683: HUMERAL REAMER SZ 3
• 00885556912676: HUMERAL REAMER SZ 2
• 00885556912669: HUMERAL REAMER SZ 1