CyberTech

GUDID 10848782029300

C17 5-0 BBS 18"/45CM

Surgical Specialties México, S. de R.L. de C.V.

Silk suture, sterile

• Primary Device ID: 10848782029300
• NIH Device Record Key: 92c6cc06-8711-4d96-8d7a-ad95add22101
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CyberTech
• Version Model Number: 900-8122
• Company DUNS: 812762226
• Company Name: Surgical Specialties México, S. de R.L. de C.V.
• Device Count: 1
• DM Exempt: true
• 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: 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(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com
• Phone: +1(877)991-1110
• Email: service@surgicalspecialties.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00848782029303 [Primary]
GS1	10848782029300 [Package]; Contains: 00848782029303; Package: Box [12 Units]; In Commercial Distribution

FDA Product Code

• GAP: SUTURE, NONABSORBABLE, SILK

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-11
• Device Publish Date: 2019-02-19

On-Brand Devices [CyberTech]

• 10848782029379: C7 3-0 BBS 18"/45CM
• 10848782029362: C7 2-0 BBS 18"/45CM
• 10848782029355: C6 4-0 BBS 18"/45CM
• 10848782029348: C6 3-0 BBS 18"/45CM
• 10848782029331: C22 5-0 BBS 18"/45CM
• 10848782029324: C22 4-0 BBS 18"/45CM
• 10848782029317: C22 3-0 BBS 18"/45CM
• 10848782029300: C17 5-0 BBS 18"/45CM
• 10848782029294: C3P 4-0 BBS 18"/45CM
• 10848782029287: T14 3-0 BBS 18"/45CM
• 10848782029270: C9 3-0 BBS 18"/45CM
• 10848782029263: C20 4-0 BBS 18"/45CM
• 10848782029256: HS16 3-0 BBS 18"/45CM
• 10848782029249: C7 3-0 VIO BR PGA 27/70
• 10848782029232: C6 4-0 VIO BR PGA 27/70
• 10848782029225: T28 4-0 VIO BR PGA 18/45
• 10848782029218: C6 4-0 UNDYED BR PGA-FA 18/45
• 10848782029201: C6 3-0 UNDYED BR PGA-FA 18/45