Isansys
by Isansys Lifecare Ltd 9 variants
Part of a family of 11 devices: see the family page
Ref Gateway SM-X205 GSM, Lifetouch Neonate, Lifetouch Neonate Snap, Lifetemp Sensor - V2 - Medium, Lifetouch Sensor - Large, Lifetouch SmallModel PSE_2
Isansys (Gateway SM-X205 GSM) is a medical device (EU MDR Class IIa; FDA Class II; FDA product code DRG, Transmitters And Receivers, Physiological Signal, Radiofrequency; EMDN category measurement devices) made by Isansys Lifecare, Ltd., registered in EUDAMED on 30 Jun 2022 (Basic UDI-DI 506048868PSE2EG), cleared under FDA 510(k) K172329 on 23 Apr 2018 and listed in FDA GUDID since 25 Apr 2024 (UDI-DI 05060488680311), active as of 22 Oct 2026.
Active
Valid until
No date given
FDA recalls
None found
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number05060488680311 | Date25 Apr 2024 | StatusListed |
| European Union | CE/MDR EUDAMED | Number506048868PSE2EG | Date30 Jun 2022 | StatusActive |
| United States | FDA 510(k)SESE GUDID | NumberK172329 | Date23 Apr 2018 | StatusActive |
Official records
- EUDAMED public site 506048868PSE2EG
- AccessGUDID record 05060488680311
- AccessGUDID record 05060488680113
- AccessGUDID record 05060488680281
- AccessGUDID record 05060488680090
- FDA 510(k) database K172329
Across registries
- EUDAMED Basic UDI-DI 506048868PSE2EG registered 30 Jun 2022 Active
- FDA 510(k) K172329 decided 23 Apr 2018 Active
- FDA GUDID UDI-DI 05060488680311 listed 25 Apr 2024 Listed
Timeline
- Cleared FDA 510(k) K172329
- Registered EUDAMED 506048868PSE2EG
- Listed FDA GUDID 05060488680311
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Isansys EUDAMEDGUDIDPatient Gateway GUDID
- Generic name
- Physiological measuring device wireless data capture/transfer unit
- Device name
- Patient Status Engine
- Model / Ref / Catalog
- PSE_2, Gateway SM-X205 GSM, Lifetouch Neonate, Lifetouch Neonate Snap, Lifetouch Sensor - Large, Lifetemp Sensor - V2 - Medium, Lifetouch Small, SM-X205 - 10.5 Screen - GSM, Lifetouch Sensor - Small
- Description
- Continuous Cardiac SensorContinuous Clinical ThermometerSM-X205 - 10.5 Screen - GSM Data entry & local display point tablet computer, 10.5 Screen
- Primary DI / UDI-DI
- 05060488680311, 05060488680076, 05060488680083, 05060488680113, 05060488680281, 05060488680090
- Basic UDI-DI
- 506048868PSE2EG
- Direct marketing DI
- 050604886803110506048868007605060488680083050604886802810506048868011305060488680090
- 510(k) Number
- FDA product code
- DRG
- EMDN code
- V0399 Measurement devices - other
- GMDN term
- Physiological measuring device wireless data capture/transfer unit
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 870.2910
- System or procedure pack
- System which is a device in itself
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class II |
Manufacturer details
- EUDAMED SRN
- GB-MF-000022154
- Authorised representative
- Isansys Lifecare Europe GmbH DE-AR-000009967
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