Identity
- Trade Name
- Womanizer FDA UDI
- Generic Name
- Sexual lubricant FDA UDI
- Model / Reference
- WZ902ALZ FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04251460630375 FDA UDI
- FDA Product Code
- NUC FDA UDI
- GMDN Term
- Sexual lubricant FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.5300 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
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Sexual lubricant
Womanizer by WOW Tech Europe GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Sexual lubricant.
- Nooky Lube Water Based Lubricant — MANO & MANO PTY. LTD. · Class II
- ID BackSlide 1oz Pocket Bottle Case of 24 — WESTRIDGE LABORATORIES INCORPORATED · Class II
- Lovehoney Cherry — WESTRIDGE LABORATORIES INCORPORATED · Class II
- LOLA — ALYK, INC. · Class II
- Wet hempation Personal Lubricant — Trigg Laboratories, Inc. · Class II
- JO H2O Flavored Peach 1oz/30ml — CC Wellness LLC · Class II
- pjur BACK DOOR Moisturizing — Pjur Group Luxembourg SA · Class II
- Lovehoney — WESTRIDGE LABORATORIES INCORPORATED · 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
- WOW Tech Europe GmbH
Sources (1)
- FDA UDI a839b0c4-9d60-41bf-8272-378330f76c0b 32 fields · synced Jun 1, 2026