Identity
- Trade Name
- UPPER LIMB KIT – 7 WISE FDA UDI
- Generic Name
- Kinesiology/electromyographic sensor set FDA UDI
- Device Name
- The Showmotion UPPER 7 kit includes 7 WISE sensors, a GATEWAY receiver, elastic bands and a charger. The platform allows to carry out the kinematic analysis of the movement of the upper district. FDA UDI
- Model / Reference
- SHWM01U7 FDA UDI
- Description
- The Showmotion UPPER 7 kit includes 7 WISE sensors, a GATEWAY receiver, elastic bands and a charger. The platform allows to carry out the kinematic analysis of the movement of the upper district. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08051122041039 FDA UDI
- FDA Product Code
- ISD FDA UDI
- GMDN Term
- Kinesiology/electromyographic sensor set FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5360 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Kinesiology/electromyographic sensor set
Upper Limb Kit – 7 Wise by Ncs Lab Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Kinesiology/electromyographic sensor set.
- BioStamp nPoint™ — Medidata Solutions, Inc. · Class II
- BioStamp® nPoint — Medidata Solutions, Inc. · Class II
- Telemyo — Noraxon USA, Inc. · Class II
- BioStamp nPoint™ — Medidata Solutions, Inc. · Class II
- TeleMyo — Noraxon USA, Inc. · Class II
- BioStamp nPoint™ — Medidata Solutions, Inc. · Class II
- BioStamp® — Medidata Solutions, Inc. · Class II
- Steadys-Step — NEUROSOFT, OOO · Class II
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ncs Lab Srl
Sources (1)
- FDA UDI e79aea0b-a112-42b7-b505-329de5d4d45f 34 fields · synced Jun 1, 2026