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Espire Elbow Pro- Right- Caucasian- Small
EUDAMEDFDA UDIClass I (EU MDR)
Ref EEP-RCS
Identity
- Trade Name
- Espire Elbow Pro- Right- Caucasian- Small EUDAMEDESPIRE FDA UDI
- Generic Name
- Electrical elbow prosthesis FDA UDI
- Device Name
- Electrical elbow prosthesis EUDAMED
- Model / Reference
- EEP-RCS EUDAMEDEspire Elbow Pro- Right- Caucasian- Small FDA UDI
Identifiers
- Catalog Number
- EEP-RCS FDA UDI
- Primary DI / UDI-DI
- 50563943283930 EUDAMED05056394328393 FDA UDI
- Basic UDI-DI
- 50553482ELE00077 EUDAMED
- 510(k) Number
- K182757 FDA UDI
- FDA Product Code
- IRE FDA UDI
- EMDN Code
- Y061899 UPPER EXTREMITY PROSTHESES - OTHER EUDAMED
- GMDN Term
- Electrical elbow prosthesis FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 890.3420 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Espire Elbow Pro- Right- Caucasian- Small by Hugh Steeper Limited — 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 | 50553482ELE00077 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Hugh Steeper Limited
- EUDAMED SRN
- GB-MF-000010196
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 48ba7922-65d4-4790-b4c6-4041930f71be 61 fields · synced Jun 18, 2026
- FDA UDI 16c5302b-fcf3-4ced-814e-07ab41e917ee 34 fields · synced May 30, 2026