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Matrix Max 2 AFO - X Large Right
EUDAMEDFDA UDIClass I (EU MDR)
Ref FH260R05
by Trulife Ltd
Identity
- Trade Name
- Matrix Max 2 AFO - X Large Right EUDAMEDMatrix Max 2 FDA UDI
- Generic Name
- Ankle/foot orthosis FDA UDI
- Device Name
- Ankle foot orthosis EUDAMEDMatrix Max 2 Trimmable AFO (X Large Right) FDA UDI
- Model / Reference
- FH260R05 EUDAMEDFDA UDI
- Description
- Matrix Max 2 Trimmable AFO (X Large Right) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00645517844886 EUDAMEDFDA UDI
- Basic UDI-DI
- 5052893CFMCQ EUDAMED
- Direct Marketing DI
- 00645517844886 EUDAMED
- FDA Product Code
- IQI FDA UDI
- EMDN Code
- Y06120602 ENERGY RETURN ANKLE-FOOT ORTHOSES EUDAMED
- GMDN Term
- Ankle/foot orthosis FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 890.3475 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Matrix Max 2 AFO - X Large Right by Trulife Ltd — 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 | 5052893CFMCQ | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Trulife Ltd
- EUDAMED SRN
- GB-MF-000015741
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (2)
- EUDAMED 0322f89c-947b-4d19-9564-9a68a11ff1ee 61 fields · synced Jun 18, 2026
- FDA UDI 1a6f4ad5-f496-4192-9e91-6b43a59326b0 33 fields · synced May 29, 2026