FDA UDI Not in Commercial Distribution 🇺🇸 United States

Sonolith i-move Standard Module

DI: 03661690000106 · Model: TMS 239269 · EDAP-TMS FRANCE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Sonolith i-move Standard Module
Primary DI
03661690000106
Version / Model
TMS 239269
Catalog Number
TMS 239269
Company Name
EDAP-TMS FRANCE
Labeler DUNS
383113362
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
5
Public Version Date
2024-12-11
Public Version Status
Update
Public Device Record Key
9abdbf26-5c98-4509-8146-f7468a1bc28d
Distribution End Date
2024-05-24

Device Description

SONOLITH® i-move medical device is a lithotripter of ESWL type (Extracorporeal Shock Wave Lithotripsy). The physical principle consists in delivering pulsed pressure waves which are focalized on the stone to be treated, at fixed frequency or patient synchronized frequency.

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
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 03661690000106

Customer Contacts

Phone
512 832-7956

Premarket Submissions

Submission Number Supplement Number
K111808 000