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Foot Pedal

FDA UDI

Class II (US FDA UDI)

by Orpheus Medical Ltd

Identity

Trade Name
Foot Pedal FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
A "2 part" medical Foot Pedal connected to the Orpheus CAST to operate: start/stop, snapshot taking. FDA UDI
Model / Reference
01 FDA UDI
Description
A "2 part" medical Foot Pedal connected to the Orpheus CAST to operate: start/stop, snapshot taking. FDA UDI

Identifiers

Catalog Number
MPU-EG00C01 FDA UDI
Primary DI / UDI-DI
07290017025063 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Foot-switch, electrical

Foot Pedal by Orpheus Medical Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot-switch, electrical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orpheus Medical Ltd

Sources (1)

  • FDA UDI 8c7dd1d2-d29c-4dce-9f69-f22fcb53437c 34 fields · synced May 30, 2026