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Matrix Max AFO (Small Left)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref FH250L02

by Trulife Ltd

Identity

Trade Name
Matrix Max AFO (Small Left) EUDAMED
Matrix Max FDA UDI
Generic Name
Ankle/foot orthosis FDA UDI
Device Name
Ankle foot orthosis EUDAMED
Matrix Max AFO (Small Left) FDA UDI
Model / Reference
FH250L02 EUDAMEDFDA UDI
Description
Matrix Max AFO (Small Left) FDA UDI

Identifiers

Primary DI / UDI-DI
00645517538112 EUDAMEDFDA UDI
Basic UDI-DI
5052893CFMCQ EUDAMED
Direct Marketing DI
00645517538112 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 AFO (Small Left) 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

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Manufacturer

Manufacturer
Trulife Ltd
EUDAMED SRN
GB-MF-000015741
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 6e35109a-6b22-4df9-91ea-4dc526462c7b 61 fields · synced Jul 12, 2026
  • FDA UDI cd04efa0-da40-4e87-bfc2-0a054bada8d7 33 fields · synced May 27, 2026