Vaxaid

FDA UDI

Class II (US FDA UDI)

by Dx Products Limited

Identity

Trade Name: Vaxaid FDA UDI
Generic Name: Penile vacuum device FDA UDI
Device Name: Vaxaid V5 Trainer FDA UDI
Model / Reference: Vaxaid V5 Trainer FDA UDI
Description: Vaxaid V5 Trainer FDA UDI

Identifiers

Catalog Number: VX-V5-T FDA UDI
Primary DI / UDI-DI: 05060140208464 FDA UDI
FDA Product Code: LKY FDA UDI
GMDN Term: Penile vacuum device FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5020 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Depth — 5 Inch FDA UDI
Lumen/Inner Diameter — 1.9 Inch FDA UDI

Category: Penile vacuum device

Vaxaid by Dx Products Limited — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Dx Products Limited

Sources (1)

FDA UDI e085d947-4b26-4f81-be99-b89413d7b1d5 36 fields · synced May 30, 2026