Identity
- Trade Name
- Podimetrics Remanufactured SmartMat FDA UDI
- Generic Name
- Temperature telemetric monitoring system FDA UDI
- Device Name
- Foot examination tool for inflammatory changes. FDA UDI
- Model / Reference
- PMHS201U-R FDA UDI
- Description
- Foot examination tool for inflammatory changes. FDA UDI
Identifiers
- Catalog Number
- PMHS201U-R FDA UDI
- Primary DI / UDI-DI
- 00866538000314 FDA UDI
- FDA Product Code
- OIZ FDA UDI
- GMDN Term
- Temperature telemetric monitoring system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Temperature telemetric monitoring system
Podimetrics Remanufactured SmartMat by Podimetrics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Temperature telemetric monitoring system.
- Podimetrics SmartMat — Podimetrics, Inc. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Podimetrics, Inc.
Sources (1)
- FDA UDI 6a2f1d3c-0af3-4ce7-a26c-d8ca60ba4d0c 36 fields · synced May 30, 2026