FDA UDI In Commercial Distribution 🇺🇸 United States

InterStim™

DI: 00763000203894 · Model: 3560022 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
InterStim™
Primary DI
00763000203894
Version / Model
3560022
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-10
Public Version
2
Public Version Date
2026-01-23
Public Version Status
Update
Public Device Record Key
8fd69010-76a3-4841-8bb2-b96ede541870

Device Description

EXT 3560022 ISTM QUAD PERC 4.32MM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
EZW Stimulator, electrical, implantable, for incontinence
QON Implanted electrical device intended for treatment of fecal incontinence

GMDN Terms

Code Name
61394 Sacral plexus percutaneous incontinence-control electrical stimulation system electrode

Identifiers

Type ID
Primary 00763000203894

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P080025 197
P970004 302

Device Sizes

Type Value Unit Text
Length 100.0 Centimeter