FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00613994752178 · Model: 3625 · MEDTRONIC, INC.
Product Codes
10
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
00613994752178
Version / Model
3625
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
5
Public Version Date
2026-01-22
Public Version Status
Update
Public Device Record Key
82a9cffc-dbc8-4287-ba05-5ba93c5a173b

Device Description

ACC 3625 SCREENER BEI REDESIGN US MKT

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
MRU implanted subcortical electrical Stimulator (motor disorders)
MHY STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
EZW Stimulator, electrical, implantable, for incontinence
GZF STIMULATOR, PERIPHERAL NERVE, IMPLANTED (PAIN RELIEF)
LGW STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
MFR Stimulator, brain, implanted, for behavior modification
NHL STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS
OLM Deep brain stimulator for obsessive compulsive disorder (OCD)
PJS Stimulator, electrical, implanted, for essential tremor
QON Implanted electrical device intended for treatment of fecal incontinence

GMDN Terms

Code Name
61392 Sacral plexus percutaneous incontinence-control electrical stimulation system pulse generator

Identifiers

Type ID
Primary 00613994752178

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P080025 020
P840001 178
P960009 108
P970004 104