Endo E0016403-1

GUDID 00885556741092

CURVED ARTHROPIERCE

Smith & Nephew, Inc.

Rigid endoscopic grasping forceps, reusable

• Primary Device ID: 00885556741092
• NIH Device Record Key: 09d070be-0139-4993-af17-4f3809672d4e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Endo
• Version Model Number: E0016403-1
• Catalog Number: E0016403-1
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556741092 [Primary]

FDA Product Code

• NBH: Accessories, arthroscopic

Sterilization

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

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

[00885556741092]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-11
• Device Publish Date: 2019-03-01

On-Brand Devices [Endo]

• 00885556741092: CURVED ARTHROPIERCE
• 00885556741962: DISTAL BICEP TENDON DRILL GUIDE
• 00885556748510: CURVED ARTHROPIERCE