Vario Foot control

FDA UDI

Class I (US FDA UDI)

by Nouvag AG

Identity

Trade Name: Vario Foot control FDA UDI
Generic Name: Foot-switch, electrical FDA UDI
Device Name: Vario Foot Control for TCM 3000 BL FDA UDI
Model / Reference: 1507NOU FDA UDI
Description: Vario Foot Control for TCM 3000 BL FDA UDI

Identifiers

Primary DI / UDI-DI: ENOU1507NOU0 FDA UDI
FDA Product Code: GEY FDA UDI
HET FDA UDI
GMDN Term: Foot-switch, electrical FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4820 FDA UDI
884.1720 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Foot-switch, electrical

Vario Foot control by Nouvag AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Nouvag AG

Sources (1)

FDA UDI 8c6a87fa-cfbb-4641-a4f0-e76bf18945ea 34 fields · synced May 30, 2026