FDA UDI Not in Commercial Distribution 🇺🇸 United States

LITHOCLAST

DI: 07613353125813 · Model: EK-386BR · E.M.S. Electro Medical Systems S.A.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
LITHOCLAST
Primary DI
07613353125813
Version / Model
EK-386BR
Catalog Number
M006840205R0
Company Name
E.M.S. Electro Medical Systems S.A.
Labeler DUNS
481233849
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-12
Public Version
4
Public Version Date
2018-12-31
Public Version Status
Update
Public Device Record Key
bdca41bc-e280-412e-82a0-c3e5f55ec681
Distribution End Date
2018-12-31

Device Description

Swiss LithoClast Trilogy Foot Switch Refurbished

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
FFK Lithotriptor, Electro-Hydraulic

GMDN Terms

Code Name
47012 Pneumatic/ultrasonic lithotripsy system

Identifiers

Type ID
Primary 07613353125813

Customer Contacts

Phone
+41229944700

Premarket Submissions

Submission Number Supplement Number
K173234 000