Identity
- Trade Name
- Dynatron TX900+ Traction System FDA UDI
- Generic Name
- Intermittent powered traction system FDA UDI
- Model / Reference
- TX900+ FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10660584000321 FDA UDI
- 510(k) Number
- K993919 FDA UDI
- FDA Product Code
- ITH FDA UDI
- GMDN Term
- Intermittent powered traction system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5900 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
Dimensions & Sizes
- Size
- Height — 10.6 Inch FDA UDIWidth — 10.6 Inch FDA UDILength — 13.4 Inch FDA UDI
Category: Intermittent powered traction system
Dynatron TX900+ Traction System by Dynatronics Corp. — 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
- Dynatronics Corp.
Sources (1)
- FDA UDI 2ab6f4d1-be0c-4753-9d9a-306f0ad77b74 36 fields · synced May 30, 2026