GUDID 00763000210205

ACCY 3550S-02 STIMLOC DISPSBL SCREWDRVER

MEDTRONIC, INC.

Neurosurgical procedure kit, non-medicated, single-use
Primary Device ID00763000210205
NIH Device Record Key528400d6-5989-46ea-bae4-877e9e3a40e2
Commercial Distribution StatusIn Commercial Distribution
Version Model Number3550S-02
Company DUNS796986144
Company NameMEDTRONIC, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000210205 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GXRCOVER, BURR HOLE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-11-01
Device Publish Date2021-10-24

Devices Manufactured by MEDTRONIC, INC.

00199150006045 - N/A2026-02-10 COMM HANDSET KIT TH90D01 DBS EMANUAL US
00199150068302 - NA2026-02-10 CUSTOM PACK BB12M12R7 HLO CPB
20199150068351 - NA2026-02-10 CUSTOM PACK 12C75R1 20PK ACC BIDMC-PCK
20199150068382 - NA2026-02-10 CUSTOM PACK BB12C41R9 10PK ACC LNG PK
00199150068869 - NA2026-02-10 CUSTOM PACK BB7V82R30 HLO L ADULT
20199150068900 - NA2026-02-10 CUSTOM PACK BB12T59R 2PK ACC STOPCOCK P
00199150068913 - NA2026-02-10 CUSTOM PACK BB11B96R6 HLO HEARTPACK
00199150068968 - NA2026-02-10 CUSTOM PACK BB8R57R10 AVL AV1/2X

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.