Identity
- Trade Name
- POLYSONIC FDA UDI
- Generic Name
- Electrode conductive medium FDA UDI
- Device Name
- Polysonic Ultrasound Lotion, one gallon bottle FDA UDI
- Model / Reference
- ULTRASOUND LOTION FDA UDI
- Description
- Polysonic Ultrasound Lotion, one gallon bottle FDA UDI
Identifiers
- Catalog Number
- 21-28 FDA UDI
- Primary DI / UDI-DI
- 00855683006319 FDA UDI
- FDA Product Code
- IYO FDA UDI
- GMDN Term
- Electrode conductive medium FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1560 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
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: Electrode conductive medium
A comprehensive review of the Polysonic Ultrasound Lotion, including its features, compliance, and FAQs.
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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
- Parker Laboratories, Inc.
Sources (1)
- FDA UDI cc5ccd00-ad11-4df6-afc5-febc86855d3e 35 fields · synced Jul 24, 2026