Identity
- Trade Name
- QB1 Go System FDA UDI
- Generic Name
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
- Device Name
- CyMedica Orthopedics QB1 Go System FDA UDI
- Model / Reference
- QB-1000-175 FDA UDI
- Description
- CyMedica Orthopedics QB1 Go System FDA UDI
Identifiers
- Catalog Number
- QB-1000-175 FDA UDI
- Primary DI / UDI-DI
- 00854816006714 FDA UDI
- GMDN Term
- Physical therapy transcutaneous neuromuscular electrical stimulation system FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 24.88 Inch FDA UDI
Category: Physical therapy transcutaneous neuromuscular electrical stimulation system
QB1 Go System by Motive Health, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Motive Health, Inc.
Sources (1)
- FDA UDI 3f1f98c7-904f-4788-9c5e-1bac6ff75b3d 37 fields · synced May 30, 2026