Identity
- Trade Name
- Midmark EUDAMEDFDA UDI
- Generic Name
- Leg procedure positioner FDA UDI
- Device Name
- Ritter 204 Manual Examination Table EUDAMEDThe Articulating Knee Crutches (without 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
- 204-013 EUDAMED9A411001 EUDAMEDFDA UDI
- Description
- The Articulating Knee Crutches (without 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
- 9A411001 FDA UDI
- Primary DI / UDI-DI
- 00841709113215 EUDAMEDFDA UDI
- Basic UDI-DI
- 00841709118708GH EUDAMED
- Direct Marketing DI
- 00841709113215 EUDAMED
- FDA Product Code
- GBB FDA UDIFRK 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 UDI880.6140 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 00841709118708GH | 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 a2edf529-16a2-4a9a-a3a6-ddbe24c5debe 61 fields · synced Jun 8, 2026
- FDA UDI 66573fa7-2937-46c5-8679-a5b0a89ba234 35 fields · synced May 30, 2026