Kit, Hand Drill, Cranial

GUDID 00643169498457

DRILL 24050 VENTRICULOSTOMY CRANIAL

MEDTRONIC PS MEDICAL, INC.

Manual surgical rotary handpiece Manual surgical rotary handpiece Manual surgical rotary handpiece, reusable Manual surgical rotary handpiece, reusable Manual surgical rotary handpiece, reusable Manual surgical rotary handpiece, reusable Manual surgical rotary handpiece, reusable Manual surgical rotary handpiece, reusable Manual surgical rotary handpiece, reusable Manual surgical rotary handpiece, reusable Manual surgical rotary handpiece, reusable

• Primary Device ID: 00643169498457
• NIH Device Record Key: 68135791-f880-4383-bcb7-33cf0b33545b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kit, Hand Drill, Cranial
• Version Model Number: 24050
• Company DUNS: 089055867
• Company Name: MEDTRONIC PS MEDICAL, 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: true
• 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)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169498457 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K904283

FDA Product Code

• HBG: DRILLS, BURRS, TREPHINES & ACCESSORIES (MANUAL)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-06-13

Devices Manufactured by MEDTRONIC PS MEDICAL, INC.

• 00763000467364 - BECKER SYSTEMS: 2024-07-01 EDMS 27931 BECKER GS TUBING SMARTSITES
• 00763000467401 - NA: 2024-06-10 CONNECTOR 9041 LUERLOCK TO FIT 1.3MM ID
• 00763000529338 - Becker External Drainage and Monitoring System: 2024-05-27 BECKER 27761 STOP BCNDLESS PATLN 24
• 00763000406073 - Becker: 2024-04-08 EDMS 46128 BECKER II BLUE PT LN
• 00763000467340 - NA: 2024-03-11 KIT 46442 EDM LUMBAR DRN CLS TIP 5PK
• 00763000406042 - NA: 2024-03-05 ASSEMBLY 46422 EDM DRAINAGE
• 00763000406080 - NA: 2024-03-05 DRAIN 27302 EDM LUMBAR W/120 GRAD CH
• 00763000431259 - Becker: 2024-03-05 EDMS 46129 EURO BECKER II BLUE PT LN