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Vapr

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
VAPR FDA UDI
Generic Name
Foot-switch, electrical FDA UDI
Device Name
VAPR 3 Footswitch REUSABLE FDA UDI
Model / Reference
225023 FDA UDI
Description
VAPR 3 Footswitch REUSABLE FDA UDI

Identifiers

Catalog Number
225023 FDA UDI
Primary DI / UDI-DI
10886705009114 FDA UDI
FDA Product Code
GEI FDA UDI
HRX FDA UDI
GMDN Term
Foot-switch, electrical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
888.1100 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

No

FDA UDI

Category: Foot-switch, electrical

Vapr by Medos International Sàrl — 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
Medos International Sàrl

Sources (1)

  • FDA UDI 074c4f7e-9952-435d-bbcf-40d63e99135b 36 fields · synced May 30, 2026