DEVICE: LITHOCLAST (07613353123574)

Device Identifier (DI) Information

LITHOCLAST
FR-289
Not in Commercial Distribution
M0068402860
E.M.S. Electro Medical Systems S.A.
07613353123574
GS1
December 31, 2018
1
481233849 *Terms of Use
Swiss LithoClast Trilogy Disposable Probe Ø1.1x425mm
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Device Characteristics

Labeling does not contain MRI Safety Information
No
No
Yes
Yes
No
No
No
No

GMDN

[?]

GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.

GMDN Term Code GMDN Term Name GMDN Term Definition GMDN Term Status [?] Implantable?
60703 Ultrasonic lithotripsy system probe, single-use
A slender, metal, tubular device that is coaxially attached to an ultrasonic lithotripsy system handpiece [a hand-held acoustic transducer that produces ultrasound (US) waves] and intended to transmit US waves to calculi (stones) in the urinary tract (i.e., kidneys, ureters, and bladder) for their fragmentation. Its distal end is brought into contact with calculi and transmits the energy, breaking down the calculi in the body for removal through its lumen. This device is introduced through the working channel of an appropriate endoscope (e.g., a percutaneous nephroscope for ureteral stones). This is a single-use device.
Active false
60461 Electrohydraulic/pneumatic lithotripsy system probe, urinary, single-use
A sterile, slender, rod-like device intended to be used as part of an intracorporeal lithotripsy system to transmit shock waves from electrohydraulic or pneumatic sources directly to a calculus in the urinary tract (i.e., kidneys, ureters, and bladder), providing high-speed fragmentation of the calculus in situ. It is typically made of high-grade stainless steel, may be rigid or semi-flexible, and is available in a variety of sizes and lengths. It may be introduced endoscopically through a natural body orifice or a surgically made opening. This is a single-use device.
Obsolete false
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FDA Product Code

[?]
Product Code Product Code Name
FFK Lithotriptor, Electro-Hydraulic
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K173234 000
No CLOSE

Sterilization

Yes
No
Sterilization Method [?]
No Sterilization Methods Found
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Storage and Handling

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
Length: 425 Millimeter
Outer Diameter: 1.1 Millimeter
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Device Record Status

36e96250-71e3-4813-b683-390815cde70d
January 08, 2021
5
March 12, 2018
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Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]
Package DI Number Quantity per Package Contains DI Package Package Discontinue Date Package Status Package Type
No Package DIs found
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
Yes
No
No CLOSE

Customer Contact

[?]
+41229944700
udi@ems-ch.com
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