Identity
- Trade Name
- KINVENT FDA UDI
- Generic Name
- Back/leg/chest dynamometer, electronic FDA UDI
- Device Name
- Bubble is a pneumatic sensor allowing you to work your strength with convenient inflatable tools. FDA UDI
- Model / Reference
- Bubble V2R01 FDA UDI
- Description
- Bubble is a pneumatic sensor allowing you to work your strength with convenient inflatable tools. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03770011995448 FDA UDI
- FDA Product Code
- LBB FDA UDI
- GMDN Term
- Back/leg/chest dynamometer, electronic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1240 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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Back/leg/chest dynamometer, electronic
Kinvent by Kinvent Hellas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Back/leg/chest dynamometer, electronic.
- Lafayette Hand-Held Dynamometer — Lafayette Instrument Company · Class I
- ActivForce 2 — ACTIVBODY · Class II
- KINVENT — KINVENT HELLAS · Class II
- KINVENT — KINVENT HELLAS · 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 |
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Manufacturer
- Manufacturer
- Kinvent Hellas
Sources (1)
- FDA UDI 69b3719c-5a76-4475-a072-4fb69d3b141e 35 fields · synced May 31, 2026