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Foot Pedal, Dual Valve

FDA UDI

Class I (US FDA UDI)

by Kdl Medical, Inc.

Identity

Trade Name
Foot Pedal, Dual Valve FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
Dual Foot Valve for VisionMist Stabilizer with Blower FDA UDI
Model / Reference
FTV-1020 FDA UDI
Description
Dual Foot Valve for VisionMist Stabilizer with Blower FDA UDI

Identifiers

Primary DI / UDI-DI
00899054002296 FDA UDI
FDA Product Code
DWS FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
870.4500 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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Foot-switch, electrical

Foot Pedal, Dual Valve by Kdl Medical, Inc. — Class I — 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
Kdl Medical, Inc.

Sources (1)

  • FDA UDI 6c59391b-f70e-42f9-991f-2e3a28076cbc 34 fields · synced May 30, 2026