← Back to catalogue

Midmark

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 204-014Model 204-013

by Midmark Corporation

Identity

Trade Name
Midmark EUDAMEDFDA UDI
Generic Name
Examination/treatment table, manual FDA UDI
Device Name
Ritter 204 Manual Examination Table EUDAMED
The Midmark 204 Manual Examination Table is intended to be used as a table to provide positioning and support of patients during examination procedures conducted by qualified medical professionals in an office environment. FDA UDI
Model / Reference
204-013 EUDAMED
204-014 EUDAMED
204 Manual Examination Table FDA UDI
Description
The Midmark 204 Manual Examination Table is intended to be used as a table to provide positioning and support of patients during examination procedures conducted by qualified medical professionals in an office environment. FDA UDI

Identifiers

Catalog Number
204-014 FDA UDI
Primary DI / UDI-DI
00841709106231 EUDAMEDFDA UDI
Basic UDI-DI
00841709118708GH EUDAMED
Direct Marketing DI
00841709106231 EUDAMED
FDA Product Code
FRK FDA UDI
EMDN Code
V080202 MANUAL MEDICAL CHAIRS EUDAMED
GMDN Term
Examination/treatment table, manual FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.6140 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 29aab88b-5fde-4a16-bf11-4f1ca16ce34f 61 fields · synced Jul 9, 2026
  • FDA UDI f0ce2040-7c26-4629-a6aa-2280e832fe2e 36 fields · synced May 30, 2026