Identity
- Trade Name
- Vertetrac FDA UDI
- Generic Name
- Wearable lumbar spine traction device FDA UDI
- Device Name
- The Vertetrac provides safe, simple, compact, and effective treatment of lumbar spine disorders and brings to both the patient and physician a means of powerful, dynamic traction with simultaneous, three-dimensional action without the need for traction beds or restrictive braces. Thus, the Vertetrac allows the patient maximum mobility with minimal restrictions or discomfort during treatment. The Vertetrac facilitates the treatment of the patient by the health service professional while also allowing chronic sufferers to administer self-treatment under qualified medical supervision. FDA UDI
- Model / Reference
- VERT9 FDA UDI
- Description
- The Vertetrac provides safe, simple, compact, and effective treatment of lumbar spine disorders and brings to both the patient and physician a means of powerful, dynamic traction with simultaneous, three-dimensional action without the need for traction beds or restrictive braces. Thus, the Vertetrac allows the patient maximum mobility with minimal restrictions or discomfort during treatment. The Vertetrac facilitates the treatment of the patient by the health service professional while also allowing chronic sufferers to administer self-treatment under qualified medical supervision. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290015711104 FDA UDI
- FDA Product Code
- IQE FDA UDI
- GMDN Term
- Wearable lumbar spine traction device FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3490 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Wearable lumbar spine traction device
Vertetrac by Meditrac Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Wearable lumbar spine traction device.
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- D.B.S. Dynamic Brace System — MEDITRAC LTD. · 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
- Meditrac Ltd.
Sources (1)
- FDA UDI 9fbd4a3a-447e-413b-968a-3c4e4124d970 33 fields · synced May 31, 2026