163005640

GUDID 10705034507415

CONCORDE Clear MIS DISCECTOMY DEVICE 6MM, 40 DEGREES

Medos International Sàrl

Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use Surgical/emergency suction cannula, non-illuminating, single-use

• Primary Device ID: 10705034507415
• NIH Device Record Key: a5fbc153-4967-4be1-a181-aad9d999cbf3
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 163005640
• Catalog Number: 163005640
• Company DUNS: 482661753
• Company Name: Medos International Sàrl
• 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: 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
• 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	10705034507415 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122861

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-10-12
• Device Publish Date: 2016-10-13

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• 10886705012374 - COR: 2024-03-27 COR Disposable Kit, 8mm
• 10886705012381 - COR: 2024-03-27 COR Disposable Kit, 10mm
• 10886705012404 - COR: 2024-03-27 COR Disposable Kit, 8mm w/Perpendicularity
• 10886705012398 - COR: 2024-03-18 COR Disposable Kit, 6mm w/Perpendicularity
• 10886705012411 - COR: 2024-03-18 COR Disposable Kit, 10mm w/Perpendicularity