← Back to catalogue

Midmark

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 9A600002Model 224-011

by Midmark Corporation

Identity

Trade Name
Midmark EUDAMEDFDA UDI
Generic Name
Arm procedure positioner, reusable FDA UDI
Device Name
Ritter Barrier-Free Power Examination Chair EUDAMED
ADA Side Rail with Articulating Arm Pad: The side rail with articulating arm pad is an ADA compliant product that is intended to assist patient access to the table and assist the patient in repositioning while on the table. In addition it is intended to properly position a patient's arm for blood pressure checks and phlebotomy procedures. FDA UDI
Model / Reference
224-011 EUDAMED
9A600002 EUDAMEDFDA UDI
Description
ADA Side Rail with Articulating Arm Pad: The side rail with articulating arm pad is an ADA compliant product that is intended to assist patient access to the table and assist the patient in repositioning while on the table. In addition it is intended to properly position a patient's arm for blood pressure checks and phlebotomy procedures. FDA UDI

Identifiers

Catalog Number
9A600002 FDA UDI
Primary DI / UDI-DI
00841709106187 EUDAMEDFDA UDI
Basic UDI-DI
00841709118685GW EUDAMED
Direct Marketing DI
00841709106187 EUDAMED
FDA Product Code
GBB FDA UDI
EMDN Code
V0880 MEDICAL SUPPORT EQUIPMENT - ACCESSORIES EUDAMED
GMDN Term
Arm procedure positioner, reusable 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

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 87ea067d-f309-410a-a688-0a33f07f0733 61 fields · synced Jul 9, 2026
  • FDA UDI 019da004-2017-40ea-8f10-121db1016a58 36 fields · synced May 30, 2026