03043007S

GUDID 10886982298829

PROTECTION SLEEVE/TIB FIX/FLEX LONG / NAILS Ø 8-11MM / STER

Synthes GmbH

Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use Orthopaedic implantation sleeve, single-use

• Primary Device ID: 10886982298829
• NIH Device Record Key: 83f6681d-4954-41c5-9c3f-07f76a34819c
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 03.043.007S
• Catalog Number: 03043007S
• Company DUNS: 486711679
• Company Name: Synthes GmbH
• Device Count: 1
• DM Exempt: true
• 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: 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886982298829 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

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: 2023-02-14
• Device Publish Date: 2023-02-06

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• 10886982344250 - NA: 2024-05-13 HOOK - 10MM UPRIGHT REDUCTION CLAMP
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• 10886982346933 - NA: 2024-05-08 EXTENDED MULTI HOLE WIRE GUIDE FOR RFNA
• 10886982346957 - NA: 2024-05-08 FNS ANGLED GUIDE 130° W/ WIDER BASE
• 10887587078359 - NA: 2024-04-16 MANDIBLE BODY REDUCTION HANDLE