InMode RF Pro system
by InMode Ltd.
Ref AG609482AModel AG613237A
InMode RF Pro system (AG609482A) is a medical device (EU MDR Class IIb) made by Inmode Ltd., registered in EUDAMED on 16 Jul 2026 (Basic UDI-DI 7290016633IRF100x92) with CE/MDR certificate 3903174CE02 valid until 1 Jul 2031, active as of 7 Nov 2026.
Active
CE MDR
Valid until
1 Jul 2031
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number3903174CE02 | Date20 Jul 2026 | StatusActive |
Official records
- EUDAMED public site 7290016633IRF100x92
Certificates
- 3903174CE02 Active
Quality management system EU MDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 20 Jul 2026
- Expires
- 1 Jul 2031
Timeline
- Registered EUDAMED 7290016633IRF100x92
- Certificate issued EUDAMED 3903174CE02
- Certificate expires EUDAMED 3903174CE02
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- IgniteRF system
- Model / reference
- AG613237A, AG609482A
- Primary DI / UDI-DI
- 17290016633662
- Basic UDI-DI
- 7290016633IRF100x92
- Direct marketing DI
- 17290016633662
- EMDN code
- X0401, X0402
- Device class
- Class IIb
- System or procedure pack
- System which is a device in itself
- EU registration type
- Standard device
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- IL-MF-000023890
- Authorised representative
- AR Experts B.V. NL-AR-000023989
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