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Performance

FDA UDI

Class II (US FDA UDI)

by Blush Novelties

Identity

Trade Name
Performance FDA UDI
Generic Name
Penile vacuum device FDA UDI
Device Name
Part Number: BL-01091. Material Type: ABS, Acrylic, Silicone. Performance VX1 is a male enhancement system that consists of a motorized pump vacuum chamber, an airtight seal and a penis ring. Batteries: AAA. FDA UDI
Model / Reference
VX1 Male Enhancement Pump System-Clear FDA UDI
Description
Part Number: BL-01091. Material Type: ABS, Acrylic, Silicone. Performance VX1 is a male enhancement system that consists of a motorized pump vacuum chamber, an airtight seal and a penis ring. Batteries: AAA. FDA UDI

Identifiers

Catalog Number
BL-01091 FDA UDI
Primary DI / UDI-DI
00853858007130 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Penile vacuum device

Performance by Blush Novelties — 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
Blush Novelties

Sources (1)

  • FDA UDI 5896efa7-4194-4ffb-b4e8-39a585484ead 34 fields · synced May 31, 2026