Identity
- Trade Name
- Neutral Cable FDA UDI
- Generic Name
- Electrocardiographic electrode, reusable FDA UDI
- Model / Reference
- CWM-930S-H37 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809495931279 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Electrocardiographic electrode, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrocardiographic electrode, reusable
Neutral Cable by Chungwoo Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrocardiographic electrode, reusable.
- GE Healthcare — SHENZHEN LAUNCH ELECTRICAL CO., LTD · Class II
- ZENIX — Zoll Medical Corporation · Class III
- SURE-LOCK — CURBELL MEDICAL PRODUCTS, INC. · Class II
- SURE-LOCK — CURBELL MEDICAL PRODUCTS, INC. · Class II
- APK — Apk Technology · Class II
- SURE-LOCK — CURBELL MEDICAL PRODUCTS, INC. · Class II
- APK — Apk Technology · Class II
- APK — Apk Technology · 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
- Chungwoo Co., Ltd.
Sources (1)
- FDA UDI a58d27f4-fcdf-4e94-a759-dfb94a82773d 33 fields · synced Jun 8, 2026