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LithoVue System

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
LithoVue System FDA UDI
Generic Name
Electrical mains power extension cable FDA UDI
Device Name
Power Cord FDA UDI
Model / Reference
M0067912000 FDA UDI
Description
Power Cord FDA UDI

Identifiers

Primary DI / UDI-DI
08714729874690 FDA UDI
FDA Product Code
FGB FDA UDI
GMDN Term
Electrical mains power extension cable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrical mains power extension cable

LithoVue System by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical mains power extension cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI c168fdd5-92b0-45f8-aa11-d2ba2b2e87a6 33 fields · synced Jun 6, 2026