FDA UDI In Commercial Distribution 🇺🇸 United States

MAGNETOLITH

DI: 07630039101350 · Model: 31500.0002 · Storz Medical AG
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MAGNETOLITH
Primary DI
07630039101350
Version / Model
31500.0002
Company Name
Storz Medical AG
Labeler DUNS
481967776
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-01
Public Version
1
Public Version Date
2021-06-09
Public Version Status
New
Public Device Record Key
2686f72e-326f-4ef6-8efa-f48c06e47444

Device Description

Equipment for the extracorporeal magnetotransduction therapy.

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
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IPF Stimulator, Muscle, Powered
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

GMDN Terms

Code Name
65318 Transcutaneous electrical stimulation electrode, reusable

Identifiers

Type ID
Primary 07630039101350

Premarket Submissions

Submission Number Supplement Number
K203710 000