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Ritter

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 224-011

by Midmark Corporation

Identity

Trade Name
Ritter EUDAMEDFDA UDI
Generic Name
General examination/treatment chair, electric FDA UDI
Device Name
Ritter Barrier-Free Power Examination Chair EUDAMED
The examination table is intended to be used as a chair / table to provide positioning and support of patients during general examination procedures conducted by medical professionals. FDA UDI
Model / Reference
224-011 EUDAMEDFDA UDI
Description
The examination table is intended to be used as a chair / table to provide positioning and support of patients during general examination procedures conducted by medical professionals. FDA UDI

Identifiers

Catalog Number
224-011 FDA UDI
Primary DI / UDI-DI
00841709106026 EUDAMEDFDA UDI
Basic UDI-DI
00841709118685GW EUDAMED
Direct Marketing DI
00841709106026 EUDAMED
FDA Product Code
GBB FDA UDI
EMDN Code
V08020101 GENERIC USE ELECTRIC MEDICAL CHAIRS EUDAMED
GMDN Term
General examination/treatment chair, electric 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

Ritter 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 bc0ad2f5-44a9-4381-b7b7-402660d689c0 61 fields · synced Jun 8, 2026
  • FDA UDI 378de01d-87a3-41a2-be4b-5f3426357de6 36 fields · synced May 30, 2026