Quickie Kit

FDA UDI

Class II (US FDA UDI)

by Blush Novelties

Identity

Trade Name: Quickie Kit FDA UDI
Generic Name: Penile ring FDA UDI
Device Name: Quickie Kit - Deep Anal - White Part Number: BL-50154 Material Type: TPE FDA UDI
Model / Reference: Quickie Kit - Deep Anal - White FDA UDI
Description: Quickie Kit - Deep Anal - White Part Number: BL-50154 Material Type: TPE FDA UDI

Identifiers

Catalog Number: BL-50154 FDA UDI
Primary DI / UDI-DI: 00853858007673 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

FDA UDI

Single Use

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

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Penile ring

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

Similar devices

Also classified as Penile ring.

Constriction Ring 12mm — KESSEL medintim GmbH · Class II
Lelo Tor 2 Black — Leloi AB · Class II
Eddie — GIDDY HOLDINGS, INC. · Class II
Eddie — GIDDY HOLDINGS, INC. · Class II
FUN FACTORY — FUN FACTORY GmbH · Class II
Lelo Pino Federal Blue — Leloi AB · Class II
Lelo Pino Black — Leloi AB · Class II
Constriction Ring 9mm — KESSEL medintim GmbH · Class II

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

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

Manufacturer

Manufacturer: Blush Novelties

Sources (1)

FDA UDI 8059b237-04a7-4b0e-bc97-91ff9c1cfd5c 34 fields · synced May 30, 2026