Identity
- Trade Name
- Midmark EUDAMEDFDA UDI
- Generic Name
- General examination/treatment chair, electric FDA UDI
- Device Name
- Ritter Barrier-Free Power Examination Chair EUDAMEDThe Midmark Assist Arms are accessories that are intended to offer patients a stable platform for accessing the table and a sense of security during positioning while on the chair and while egressing from the chair. FDA UDI
- Model / Reference
- 224-011 EUDAMED9A615001 EUDAMEDFDA UDI
- Description
- The Midmark Assist Arms are accessories that are intended to offer patients a stable platform for accessing the table and a sense of security during positioning while on the chair and while egressing from the chair. FDA UDI
Identifiers
- Catalog Number
- 9A615001 FDA UDI
- Primary DI / UDI-DI
- 00841709117992 EUDAMEDFDA UDI
- Basic UDI-DI
- 00841709118685GW EUDAMED
- Direct Marketing DI
- 00841709117992 EUDAMED
- FDA Product Code
- GBB FDA UDI
- EMDN Code
- V0880 MEDICAL SUPPORT EQUIPMENT - ACCESSORIES 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
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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 00841709118685GW | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Midmark Corporation
- EUDAMED SRN
- US-MF-000002581
- Authorised Representative
- CEpartner4U NL-AR-000000111
Sources (2)
- EUDAMED f7ab7a14-44e3-40a8-9609-804715d2a0ea 61 fields · synced Jul 14, 2026
- FDA UDI 3c37ecd9-5ba6-45bb-9633-fdb834e09554 35 fields · synced May 30, 2026