ACCESSORY 3550-16 ANCHOR,BUMPY,DOMESTIC Medical Device Identification

GUDID 00681490518031

Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use

Primary Device ID	00681490518031
NIH Device Record Key	11eed723-4c42-4cca-a454-e960308543a1
Commercial Distribution Discontinuation	2018-09-26
Commercial Distribution Status	Not in Commercial Distribution
Version Model Number	3550-16
Company DUNS	796986144
Company Name	MEDTRONIC, 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

Device Issuing Agency	Device ID
GS1	00681490518031 [Primary]

LGW	STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

Steralize Prior To Use	false
Device Is Sterile	true