FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00763000517182 · Model: A51300 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
00763000517182
Version / Model
A51300
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-04
Public Version
2
Public Version Date
2026-01-21
Public Version Status
Update
Public Device Record Key
8461d938-070f-48f1-8ab6-f1c926f79554

Device Description

SW APP A51300 OASIS CLINICIAN GU

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
No
Has Lot/Batch Number
Yes
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
61393 Multiple active implantable device programmer

Identifiers

Type ID
Primary 00763000517182

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P080025 235
P970004 340