Identity
- Trade Name
- Nixit FDA UDI
- Generic Name
- Sexual lubricant FDA UDI
- Device Name
- Natural Personal Lubricant 4 fl. oz. FDA UDI
- Model / Reference
- Nixit Natural Lubricant FDA UDI
- Description
- Natural Personal Lubricant 4 fl. oz. FDA UDI
Identifiers
- Catalog Number
- 70004 FDA UDI
- Primary DI / UDI-DI
- 00627987071429 FDA UDI
- FDA Product Code
- NUC FDA UDIKMJ FDA UDI
- GMDN Term
- Sexual lubricant FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.5300 FDA UDI880.6375 FDA UDI
- Commercial Distribution
- Not 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
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 — 4 Fluid Ounce FDA UDI
Nixit by Mayer Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Mayer Laboratories
Sources (1)
- FDA UDI 0a678129-e4e0-4e3c-a8c5-81e389fdf6f0 36 fields · synced May 30, 2026