FDA UDI In Commercial Distribution 🇺🇸 United States

MODULITH®

DI: 07630039100902 · Model: SLK · Storz Medical AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MODULITH®
Primary DI
07630039100902
Version / Model
SLK
Catalog Number
30000
Company Name
Storz Medical AG
Labeler DUNS
481967776
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-28
Public Version
1
Public Version Date
2019-11-05
Public Version Status
New
Public Device Record Key
f005dd50-1efd-4d94-be68-abaa05308565

Device Description

Equipment for the extracorporeal induced shock wave therapy for stationary and mobile use.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LNS Lithotriptor, Extracorporeal Shock-Wave,Urological

GMDN Terms

Code Name
18415 Electromechanical lithotripsy system, extracorporeal

Identifiers

Type ID
Primary 07630039100902

Premarket Submissions

Submission Number Supplement Number
K120769 000