Myoblate™
by RF Medical Co., Ltd. 17 variants
Ref BTM 2530QModel BT Series
Active
CE MDR
Valid until
21 Sep 2028
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number880014291604BD 08809295140468 | Date10 Jul 2026 | StatusActive |
Certificates
- KR23/00000154 Active
Quality management system EU MDR
- Certifier
- SGS Belgium NV 1639
- Issued
- 23 Apr 2026
- Expires
- 21 Sep 2028
- Reason
- Other
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Big-Tip, MYOBLATE™
- Model / Reference
- BT Series, BTM 2530Q
- Primary DI / UDI-DI
- 08809295140468
- Basic UDI-DI
- 880014291604BD
- EMDN Code
- K0201010301 Open electrosurgery electrodes, single-use
- Device Class
- Class IIb
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- KR-MF-000012647
- Authorised representative
- Obelis s.a. BE-AR-000000106
Other devices from RF Medical Co., Ltd.
Properties
Other properties (12)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No