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Carbon Fiber Foot Plate

EUDAMEDFDA UDI

Class I (EU MDR)

Ref RMEM11

by Thrive Orthopedics

Identity

Trade Name
Thrive Orthopedics FDA UDI
Generic Name
Ankle/foot orthosis FDA UDI
Device Name
Carbon Fiber Foot Plate EUDAMED
Morton's Extension Carbon Fiber Foot Plate - 1.3 mm - US W12 | M11 FDA UDI
Model / Reference
RMEM11 EUDAMEDFDA UDI
Description
Morton's Extension Carbon Fiber Foot Plate - 1.3 mm - US W12 | M11 FDA UDI

Identifiers

Primary DI / UDI-DI
00810079191161 EUDAMEDFDA UDI
Basic UDI-DI
0081007919XGCFIS8 EUDAMED
FDA Product Code
IQI FDA UDI
EMDN Code
Y06120601 PASSIVE 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
Sweden 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ankle/foot orthosis

Carbon Fiber Foot Plate by Thrive Orthopedics — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thrive Orthopedics
EUDAMED SRN
US-MF-000026394
Authorised Representative
Code of Practice AB SE-AR-000003002

Sources (2)

  • EUDAMED 0c002b4e-2348-48cf-af49-39f68c36a567 61 fields · synced Jul 20, 2026
  • FDA UDI f6f41c34-1b80-40dc-99f2-b23fcb33a561 33 fields · synced May 29, 2026