Identity
- Trade Name
- J-stim FDA UDI
- Generic Name
- Analgesic transcutaneous electrical nerve stimulation system FDA UDI
- Device Name
- The J-Stim external, non-invasive, non-narcotic, electrotherapy system is indicated for use as an adjunctive therapy in reducing the level of pain and symptoms associated with osteoarthritis of the knee and for overall improvement of the knee. The J-Stim is also indicated for use as an adjunctive therapy in reducing the level of pain, and stiffness associated with pain, from rheumatoid arthritis of the hand. FDA UDI
- Model / Reference
- J-stim FDA UDI
- Description
- The J-Stim external, non-invasive, non-narcotic, electrotherapy system is indicated for use as an adjunctive therapy in reducing the level of pain and symptoms associated with osteoarthritis of the knee and for overall improvement of the knee. The J-Stim is also indicated for use as an adjunctive therapy in reducing the level of pain, and stiffness associated with pain, from rheumatoid arthritis of the hand. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06942808291034 FDA UDI
- FDA Product Code
- NYN FDA UDI
- GMDN Term
- Analgesic transcutaneous electrical nerve stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5890 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
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
Category: Analgesic transcutaneous electrical nerve stimulation system
J-stim by EasyMed Instruments Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Analgesic transcutaneous electrical nerve stimulation system.
- AVCOO — ADP HEALTH LIMITED · Class II
- AUVON — Shenzhen Yuwen E-Commerce Co., Ltd. · Class II
- HTG Life — FRAMEWERK LLC · Class II
- AUVON — Shenzhen Yuwen E-Commerce Co., Ltd. · Class II
- 1byone — 1BYONEPRODUCTS INC. · Class II
- AUVON — Shenzhen Yuwen E-Commerce Co., Ltd. · Class II
- Famidoc — FAMIDOC USA, INC. · Class II
- COMPEX — DJO, LLC · 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
- EasyMed Instruments Co., Ltd.
Sources (1)
- FDA UDI b3d00973-8a6d-482f-98e8-e71c2b677085 33 fields · synced May 29, 2026