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Flexible Probe

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Flexible Probe FDA UDI
Generic Name
Ultrasonic lithotripsy system probe, single-use FDA UDI
Device Name
Flexible Probe FDA UDI
Model / Reference
M0068407390 FDA UDI
Description
Flexible Probe FDA UDI

Identifiers

Catalog Number
M0068407390 FDA UDI
Primary DI / UDI-DI
08714729430599 FDA UDI
FDA Product Code
FFK FDA UDI
GMDN Term
Ultrasonic lithotripsy system probe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4480 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ultrasonic lithotripsy system probe, single-use

Flexible Probe by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasonic lithotripsy system probe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 7d1ccd72-7dad-4662-a22d-35ef732f7593 35 fields · synced May 30, 2026