TWINFIX / DURABRAID 7210294

GUDID 03596010533838

TWINFXTI2.8 STR ANCHR W/DURBRD STR 2-0

Smith & Nephew, Inc.

Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 03596010533838
• NIH Device Record Key: a97fd68c-187d-4aff-bc5a-71792da807b2
• Commercial Distribution Discontinuation: 2017-04-03
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: TWINFIX / DURABRAID
• Version Model Number: 7210294
• Catalog Number: 7210294
• Company DUNS: 045483575
• Company Name: Smith & Nephew, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: 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)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	03596010533838 [Primary]

FDA Product Code

• JDR: STAPLE, FIXATION, BONE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2023-09-07
• Device Publish Date: 2015-08-30

On-Brand Devices [TWINFIX / DURABRAID]

• 03596010585974: TWINFIX AB 6.5 SUTR ANCR W/2 DURABRAID
• 03596010584489: TWINFIX TI 2.8 HS SUTR ANCHR W/2 28 DUR
• 03596010498502: TWNFX AB 6.5 STR ANCHR2 38 DRBRD STR ND
• 03596010485656: TWINFIX TI 5.0 SUTURE ANCHOR W/TWO 38
• 03596010498496: TWNFX AB 6.5 STR ANCHR 2 38 DB STR
• 03596010001238: TWNFIX AB 6.5 STR ANCHR 2 DRBRD 38
• 03596010495440: TWNFX TI 6.5 SUTURE ANCHOR WITH TWO 38
• 03596010533838: TWINFXTI2.8 STR ANCHR W/DURBRD STR 2-0