FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00643169953635 · Model: 3550-02 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00643169953635
Version / Model
3550-02
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-29
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
0b9c0e34-41ca-4de7-a560-cb5c6c62e7aa

Device Description

ACCY 3550-02 WRENCH AND SCREWS US

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GZB STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF)
GZF STIMULATOR, PERIPHERAL NERVE, IMPLANTED (PAIN RELIEF)

GMDN Terms

Code Name
44063 Neurosurgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 00643169953635

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K960631 000