Identity
- Trade Name
- ESPIRE FDA UDI
- Generic Name
- Electrical elbow prosthesis FDA UDI
- Model / Reference
- Espire Battery Charger- Single Bay- US FDA UDI
Identifiers
- Catalog Number
- EE-CH-1US FDA UDI
- Primary DI / UDI-DI
- 05056394326030 FDA UDI
- FDA Product Code
- IRE FDA UDI
- GMDN Term
- Electrical elbow prosthesis FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3420 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrical elbow prosthesis
Espire by Hugh Steeper Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrical elbow prosthesis.
- ESPIRE — HUGH STEEPER LIMITED · Class I
- ESPIRE — HUGH STEEPER LIMITED · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hugh Steeper Limited
Sources (1)
- FDA UDI 68d66e9b-395b-4e4f-9841-73cc63c5a1b6 33 fields · synced Jun 8, 2026