Identity
- Trade Name
- TM "Rehabilitimed" L-4M-2 S Comfort FDA UDI
- Generic Name
- Multiple spinal region orthosis FDA UDI
- Device Name
- The beige orthopedic device for the lumbar spine, 24 cm high, is made of elastic bandage fabric and multilayer material (special velor fabric tripled (glued in a special way with polyurethane foam) with cotton terry cloth), which, together with stiffening ribs (metal ribs) and additional ties, allows you to provide reliable support for the lumbar spine, taking the form of lumbar lordosis. FDA UDI
- Model / Reference
- L-4M-2 S Comfort FDA UDI
- Description
- The beige orthopedic device for the lumbar spine, 24 cm high, is made of elastic bandage fabric and multilayer material (special velor fabric tripled (glued in a special way with polyurethane foam) with cotton terry cloth), which, together with stiffening ribs (metal ribs) and additional ties, allows you to provide reliable support for the lumbar spine, taking the form of lumbar lordosis. FDA UDI
Identifiers
- Catalog Number
- L-4M-2 S Comfort FDA UDI
- Primary DI / UDI-DI
- 04823097719626 FDA UDI
- FDA Product Code
- MRI FDA UDI
- GMDN Term
- Multiple spinal region orthosis 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Multiple spinal region orthosis
TM "Rehabilitimed" L-4M-2 S Comfort by Reabilitimed Tov — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Reabilitimed Tov
Sources (1)
- FDA UDI 54538409-af57-4f6e-ae0a-f7c13c1bebcf 36 fields · synced Jun 7, 2026