KANEDA SR 3210743

GUDID 10705034005270

KANEDA SR ANTERIOR SYSTEM PLATE HOLDER

Medos International Sàrl

Orthopaedic implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable

• Primary Device ID: 10705034005270
• NIH Device Record Key: 883561eb-7372-4081-840f-8f1bba712a55
• Commercial Distribution Discontinuation: 2018-07-31
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: KANEDA SR
• Version Model Number: 3210743
• Catalog Number: 3210743
• Company DUNS: 482661753
• Company Name: Medos International Sàrl
• Device Count: 1
• DM Exempt: false
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034005270 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

[10705034005270]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2020-04-06
• Device Publish Date: 2016-12-31

On-Brand Devices [KANEDA SR]

• 10705034005270: KANEDA SR ANTERIOR SYSTEM PLATE HOLDER
• 10705034005232: KANEDA SR ANTERIOR SYSTEM ANGLED AWL (MODULAR)
• 10705034005225: KANEDA SR ANTERIOR SYSTEM AWL (MODULAR)