FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00643169953598 · Model: 355038 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00643169953598
Version / Model
355038
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-30
Public Version
3
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
5f51c24d-6931-4822-bba4-090bd49e8efa

Device Description

ACCY 355038 1X8 38CM TUNNELING TOOL

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

GMDN Terms

Code Name
46801 Subcutaneous tunneller, single-use

Identifiers

Type ID
Primary 00643169953598

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P840001 377