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Bathmate

FDA UDI

Class II (US FDA UDI)

by Dx Products Limited

Identity

Trade Name
Bathmate FDA UDI
Generic Name
Penile vacuum device FDA UDI
Device Name
Bathmate Hydro 5 Aqua Blue FDA UDI
Model / Reference
Hydro 5 Aqua Blue FDA UDI
Description
Bathmate Hydro 5 Aqua Blue FDA UDI

Identifiers

Catalog Number
BM-H5-AB FDA UDI
Primary DI / UDI-DI
05060140208310 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Dimensions & Sizes

Size
Lumen/Inner Diameter — 2 Inch FDA UDI
Depth — 5 Inch FDA UDI

Category: Penile vacuum device

Bathmate by Dx Products Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Penile vacuum device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dx Products Limited

Sources (1)

  • FDA UDI 7e02aca2-2029-48dd-8391-7a6eb62d05aa 36 fields · synced May 30, 2026