MAGNUMWIRE OM-9043

GUDID 20817470007279

MAGNUMWIRE SUTURE CO-BRAID

Smith & Nephew, Inc.

Arthroscopic suturing unit

• Primary Device ID: 20817470007279
• NIH Device Record Key: 1f58000c-c6da-4ce8-b296-e99492846ed6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAGNUMWIRE
• Version Model Number: OM-9043
• Catalog Number: OM-9043
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• 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	00817470007275 [Primary]
GS1	20817470007279 [Package]; Contains: 00817470007275; Package: BX [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070673

FDA Product Code

• GAT: SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-11-13

On-Brand Devices [MAGNUMWIRE]

• 20817470007309: MAGNUMWIRE BLACK COBRAID SUTURE W NEEDLE
• 20817470007293: LOOSE MAGNUMWIRE SUTURE CO-BRAID WITH 26
• 20817470007286: LOOSE MAGNUMWIRE SUTURE WHITE WITH 26 MM
• 20817470007279: MAGNUMWIRE SUTURE CO-BRAID
• 20817470007262: MAGNUMWIRE SUTURE BLACK 12 PER BOX
• 20817470007255: MAGNUMWIRE SUTURE WHITE 12 PER BOX
• 00817470005936: MAGNUMWIRE SURGICAL SCISSOR PKG