HEALICOIL / ULTRABRAID 72203379

GUDID 00885554026306

HEALICOIL SA PK 5.5MM W/2 UB-BL CBRD BL

Smith & Nephew, Inc.

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 00885554026306
• NIH Device Record Key: 8c175a25-b234-4e63-baa7-2cbf5dfeecf2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HEALICOIL / ULTRABRAID
• Version Model Number: 72203379
• Catalog Number: 72203379
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885554026306 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113294

FDA Product Code

• MBI: FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-08-29

On-Brand Devices [HEALICOIL / ULTRABRAID]

• 00885554031416: HEALICOIL RG SA 5.5MM W/2 UB-BL CBRD BL
• 00885554030860: HEALICOIL RG SA 5.5MM W/3 UB-BL CB BL BK
• 00885554026313: HEALICOIL SA PK 5.5MM W/3 UB-BL CBBL LT
• 00885554026306: HEALICOIL SA PK 5.5MM W/2 UB-BL CBRD BL
• 03596010657862: HEALICOIL SA PK 4.5MM W/2 UB-BL CBRD BL