Identity
- Trade Name
- Autoblow Cleaner 8.1oz FDA UDI
- Generic Name
- Sexual lubricant FDA UDI
- Device Name
- Autoblow Cleaner 8.1oz FDA UDI
- Model / Reference
- Autoblow Cleaner 8.1oz FDA UDI
- Description
- Autoblow Cleaner 8.1oz FDA UDI
Identifiers
- Catalog Number
- IDD11E03 FDA UDI
- Primary DI / UDI-DI
- 00704751345327 FDA UDI
- 510(k) Number
- K051295 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
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
Category: Sexual lubricant
A comprehensive medical device directory, providing detailed information on the Autoblow Cleaner 8.1oz. This product is designed for lubrication purposes and is intended for use in obstetrics and gynecology.
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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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Westridge Laboratories Incorporated
Sources (1)
- FDA UDI 1b9a879c-dfd5-4080-8b38-b01a025c42b2 36 fields · synced Jul 23, 2026