Identity
- Trade Name
- Aqua Lube FDA UDI
- Generic Name
- Sexual lubricant FDA UDI
- Device Name
- Personal Lubricant 144 ct FDA UDI
- Model / Reference
- Aqua Lube Natural Packets FDA UDI
- Description
- Personal Lubricant 144 ct FDA UDI
Identifiers
- Catalog Number
- 51025 FDA UDI
- Primary DI / UDI-DI
- 00016169510250 FDA UDI
- 510(k) Number
- K110325 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 3 Fluid Ounce FDA UDI
Category: Sexual lubricant
Aqua Lube by Mayer Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Mayer Laboratories
Sources (1)
- FDA UDI 71cb2c87-8849-40e2-b614-13c714b7d506 38 fields · synced May 30, 2026