← Back to catalogue

Performance

FDA UDI

Class II (US FDA UDI)

by Blush Novelties

Identity

Trade Name
PERFORMANCE FDA UDI
Generic Name
Penile ring FDA UDI
Device Name
Performance - VX101 Male Enhancement Pump - Blue Part Number: BL-01102 Material Type: TPE FDA UDI
Model / Reference
Performance - VX101 Male Enhancement Pump - Blue FDA UDI
Description
Performance - VX101 Male Enhancement Pump - Blue Part Number: BL-01102 Material Type: TPE FDA UDI

Identifiers

Catalog Number
BL-01102 FDA UDI
Primary DI / UDI-DI
00853858007680 FDA UDI
FDA Product Code
LKY FDA UDI
GMDN Term
Penile ring 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 ring

Performance by Blush Novelties — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Penile ring.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Blush Novelties

Sources (1)

  • FDA UDI 269585f8-6534-49ce-958c-15d6c943f333 34 fields · synced Jun 8, 2026