Revolution Apex Select
by Ge Hangwei Medical Systems Co., Ltd. China EUDAMEDGUDID
Ref Power Xtream: B7919QT; Power Pro: B7919QS Product code JAKEMDN Z11030606
Regulatory status
Recall ongoing. 11 ongoing FDA recalls. See recalls
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number8406821BUG00213GX | Date14 Mar 2022 | StatusActive |
| United States | GUDID listing GUDID | Number00195278469700 | Date4 Feb 2022 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Recalls
-
- Ongoing Z-2153-2026
- Ongoing Z-2155-2026
- Ongoing Z-2151-2026
- Ongoing Z-2154-2026
- Ongoing Z-2152-2026
- Ongoing Z-2150-2026
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
-
- Ongoing Z-1300-2025
- Ongoing Z-1303-2025
- Ongoing Z-1298-2025
- Ongoing Z-1301-2025
- Ongoing Z-1297-2025
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.
Specification
- Trade Name
- Revolution Apex Select EUDAMEDRevolution GUDID
- Generic Name
- Full-body CT system
- Model / Ref / Catalog
- Power Xtream: B7919QT EUDAMEDPower Pro: B7919QS EUDAMEDApex Select GUDIDB7919QT-B7919QS GUDID
- Primary DI / UDI-DI
- 00195278469700
- Basic UDI-DI
- 8406821BUG00213GX
- 510(k) Number
- FDA Product Code
- JAK
- EMDN Code
- Z11030606 Computed tomographs - 128 layers or more but less than 256 layers
- GMDN Term
- Full-body CT system
- Device Class
- Class IIb EUDAMEDClass II GUDID
- Regulation Number
- 892.1750
- Market of Registration
- Belgium
- Commercial Distribution
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / Reference | Power Xtream: B7919QT; Power Pro: B7919QS | Apex Select |
| Device Class | Class IIb | Class II |
Manufacturer details
- EUDAMED SRN
- CN-MF-000009292
- Authorised representative
- GE Medical Systems SCS FR-AR-000000344
Other devices from Ge Hangwei Medical Systems Co., Ltd.
Properties & raw data
Show properties, registry sources and raw records
Other properties (21)
- Sterile: No
- Single Use: No
- 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
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
- Manufacturing Date: No
Sources (2)
- EUDAMED 4facd1c6-90e7-4c75-b43e-3d28fbe56374
- FDA UDI fa30517e-9a5e-44f5-aa29-966f6b32988c