Identity
- Trade Name
- 2-Pin Dispersive Electrode cable FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reusable FDA UDI
- Device Name
- 2-Pin connecting cable for dispersive electrode FDA UDI
- Model / Reference
- GC-2P FDA UDI
- Description
- 2-Pin connecting cable for dispersive electrode FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809295145777 FDA UDI
- 510(k) Number
- K180999 FDA UDI
- FDA Product Code
- GEI FDA UDI
- GMDN Term
- Electrical-only medical device connection cable, 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: Electrical-only medical device connection cable, reusable
2-Pin Dispersive Electrode cable by RF Medical Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrical-only medical device connection cable, reusable.
- Unimed — Unimed Medical Supplies, Inc. · Class II
- Guenter Bissinger Medizintechnik GmbH — Günter Bissinger Medizintechnik GmbH · Class II
- Unimed — Unimed Medical Supplies, Inc. · Class II
- Symmetry Olsen — Olsen Medical · Class II
- Connection Cable — Shenzhen Keborui Electronics Co., Ltd · Class I
- TC-HEART LUNG DIN INTFC CA STOCKET — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- MICTEC CONNECTION CABLE — SONTEC INSTRUMENTS, INC. · Class II
- ECG Cable — Edan Instruments,Inc. · Class I
Cleared under the same submission
K180999 also covers:
- Cooling pump — RF Medical Co., Ltd.
- Dual Foot Switch — RF Medical Co., Ltd.
- RF ABLATION SYSTEM V-1000 — RF Medical Co., Ltd.
- RFT Electrode — RF Medical Co., Ltd.
- RFT Electrode — RF Medical Co., Ltd.
- RFT Electrode — RF Medical Co., Ltd.
- RFT Electrode — RF Medical Co., Ltd.
- RFT Electrode — RF Medical Co., Ltd.
- RFT Electrode — RF Medical Co., Ltd.
- Single channel Foot Switch — RF Medical Co., Ltd.
- THYBLATE™ — RF Medical Co., Ltd.
- THYBLATE™ — RF Medical Co., Ltd.
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
- RF Medical Co., Ltd.
Sources (1)
- FDA UDI 7eea85c3-17aa-4808-a621-5ba6b7fb55d0 35 fields · synced May 30, 2026