Diagnostic Ultrasound System Cus-AME00
by Canon Inc.
Ref CUS-AME00Model CUS-ABE00, CUS-AME00, TUS-AI900, etc.
Active
CE MDR
Valid until
Not listed
FDA recalls
None foundDocuments
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number4987670A0401RF 04987670105937 | Date28 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04987670105937 | Date1 Jun 2026 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Diagnostic Ultrasound System
- Generic Name
- General-purpose ultrasound imaging system
- Model / Reference
- CUS-AME00, CUS-ABE00, TUS-AI900, etc.
- Primary DI / UDI-DI
- 04987670105937
- Basic UDI-DI
- 4987670A0401RF
- 510(k) Number
- FDA Product Code
- IYN, IYO, ITX
- EMDN Code
- Z11040104 Multidisciplinary ultrasound scanners (internal and cardiology, etc.)
- GMDN Term
- General-purpose ultrasound imaging system
- Device Class
- Class IIa EUDAMEDClass II GUDID
- Regulation Number
- 892.1550, 892.1560, 892.1570
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class II |
Other devices from Canon Inc.
Properties
Other properties (22)
- 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
- Prescription Use: 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