FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00763000869359 · Model: CD9000A · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00763000869359
Version / Model
CD9000A
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-06
Public Version
4
Public Version Date
2025-09-26
Public Version Status
Update
Public Device Record Key
2940e602-02c1-4eac-bd74-ee4291d10b72

Device Description

CHARGING DOCK CD9000A GLBL CD9000A02N

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EZW Stimulator, electrical, implantable, for incontinence
QON Implanted electrical device intended for treatment of fecal incontinence

GMDN Terms

Code Name
34158 Secondary battery

Identifiers

Type ID
Primary 00763000869359

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P080025 280
P970004 385