Identity
- Trade Name
- 6M EUDAMEDTRITON 6M EUDAMEDTRITON 6 M (SZER. 70) FDA UDI
- Generic Name
- Body arch traction table FDA UDI
- Device Name
- Stół do trakcji EUDAMEDTRITON DTS® 6M is designed to support a patient and the therapist in traction treatment. The table surface may consist of sections that can be raised and lowered to manipulate the curvature of the patient’s spine and traction accessories for lumbar and cervical traction. FDA UDI
- Model / Reference
- TRITON 6M, 6E EUDAMED- EUDAMED01-STO-3610-002 FDA UDI
- Description
- TRITON DTS® 6M is designed to support a patient and the therapist in traction treatment. The table surface may consist of sections that can be raised and lowered to manipulate the curvature of the patient’s spine and traction accessories for lumbar and cervical traction. FDA UDI
Identifiers
- Catalog Number
- 4769M FDA UDI
- Primary DI / UDI-DI
- 05903684803231 EUDAMEDFDA UDI
- Basic UDI-DI
- 590368480M065C3 EUDAMED
- FDA Product Code
- INQ FDA UDI
- EMDN Code
- Z120602 PHYSIOTHERAPY EQUIPMENT EUDAMED
- GMDN Term
- Body arch traction table FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 890.3760 FDA UDI
- Market of Registration
- Poland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
6m by Meden Inmed Sp Z O O — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 590368480M065C3 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Meden-Inmed Sp. Z O.o.
- EUDAMED SRN
- PL-MF-000001670
Sources (3)
- EUDAMED 37832dd1-ecc5-4eb1-b277-f5cc5ba50f9e 61 fields · synced Oct 6, 2026
- FDA UDI 666d10fa-30a7-4694-a583-481fdbf3d62f 34 fields · synced May 30, 2026
- EUDAMED 712cda0a-75ef-4620-b557-9bb2647e2902 61 fields · synced Jul 25, 2026