Identity
- Trade Name
- Decompression of Choice FDA UDI
- Generic Name
- Programmable powered traction system FDA UDI
- Device Name
- tower decompression table, 115V FDA UDI
- Model / Reference
- E9022 FDA UDI
- Description
- tower decompression table, 115V FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00852753008921 FDA UDI
- FDA Product Code
- ITH FDA UDI
- GMDN Term
- Programmable 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
No
FDA UDI
Category: Programmable powered traction system
Decompression of Choice by Pivotal Health Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Programmable powered traction system.
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- Decompression of Choice — Pivotal Health Solutions · Class II
- Decompression of Choice — Pivotal Health Solutions · Class II
- SpineMED Decompression System — Universal Pain Technology Canada Inc · Class II
- SpineMED Decompression System — Universal Pain Technology Canada Inc · Class II
- SpineMED Decompression System — Universal Pain Technology Canada Inc · Class II
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
- Pivotal Health Solutions, Inc.
Sources (1)
- FDA UDI 3fc01161-e508-41d3-b44a-b80a5da0fb5a 33 fields · synced Jun 8, 2026