Vysis
by Abbott Molecular Inc. 6 variants
Ref 04N60-020
Vysis (04N60-020) is a device classified as IVD General made by Abbott Molecular, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-00884999009288), active as of 7 Nov 2026.
Active
CE IVDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDD | NumberB-00884999009288 00884999009288 | Date5 Nov 2026 | StatusActive |
Official records
- EUDAMED public site B-00884999009288
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/IVDD Active
Specification
- Device name
- Vysis 1p36/1q25 and 19q13/19p13 FISH Probe Kit
- Model / reference
- 04N60-020
- Primary DI / UDI-DI
- 00884999009288
- Basic UDI-DI
- B-00884999009288
- EMDN code
- W01060299 Tests for acquired genetic or chromosomal alterations - other
- Device class
- Class IVD General
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- US-MF-000017776
- Authorised representative
- Abbott GmbH DE-AR-000009457
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