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Midmark

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9A645001Model 224-011

by Midmark Corporation

Identity

Trade Name
Midmark EUDAMEDFDA UDI
Generic Name
Leg procedure positioner FDA UDI
Device Name
Ritter Barrier-Free Power Examination Chair EUDAMED
The Articulating Knee Crutch Kit (with accessory receiver) is designed to be a more ergonomic and comfortable option compared to standard stirrups. The unique ball-socket design allows for a maximum range of adjustment, designed to ensure optimum knee and leg support. FDA UDI
Model / Reference
224-011 EUDAMED
9A645001 EUDAMEDFDA UDI
Description
The Articulating Knee Crutch Kit (with accessory receiver) is designed to be a more ergonomic and comfortable option compared to standard stirrups. The unique ball-socket design allows for a maximum range of adjustment, designed to ensure optimum knee and leg support. FDA UDI

Identifiers

Catalog Number
9A645001 FDA UDI
Primary DI / UDI-DI
00841709113277 EUDAMEDFDA UDI
Basic UDI-DI
00841709118685GW EUDAMED
Direct Marketing DI
00841709113277 EUDAMED
FDA Product Code
GBB FDA UDI
EMDN Code
V0880 MEDICAL SUPPORT EQUIPMENT - ACCESSORIES EUDAMED
GMDN Term
Leg procedure positioner FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4960 FDA UDI
Market of Registration
Netherlands 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

Midmark by Midmark Corporation — 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
Midmark Corporation
EUDAMED SRN
US-MF-000002581
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (2)

  • EUDAMED 525692bd-02e8-469a-9fae-fface389a568 61 fields · synced Jul 21, 2026
  • FDA UDI 425fc893-9a50-46dd-84f7-9e04010a719d 35 fields · synced May 30, 2026