ZCT1000240
by Johnson & Johnson Surgical Vision, Inc.
Ref ZCT1000240, ZCT4000240, ZCT6000240, ZCT1000250, ZCT1000290Model ZCT100, ZCT400, ZCT600
ZCT1000240 is a Class IIb device made by Johnson & Johnson Surgical Vision, Inc., registered in EUDAMED on 3 Mar 2026 (Basic UDI-DI B-USMF0000389680004446G), active as of 7 Nov 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-USMF0000389680004446G | Date3 Mar 2026 | StatusActive |
Official records
- EUDAMED public site B-USMF0000389680004446G
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Model / reference
- ZCT100, ZCT1000240, ZCT400, ZCT4000240, ZCT600, ZCT6000240, ZCT1000250, ZCT1000290
- Primary DI / UDI-DI
- D-USMF0000389680004446G, D-USMF0000389680010345Y, D-USMF0000389680008577D, D-USMF0000389680004466L, D-USMF0000389680004546K
- Basic UDI-DI
- B-USMF0000389680004446G, B-USMF0000389680010345Y, B-USMF0000389680008577D, B-USMF0000389680004466L, B-USMF0000389680004546K
- EMDN code
- P030102090301 IOLs, APHAKIC, MONOFOCAL, TORIC, HYDROPHOBIC ACRYLIC
- Device class
- Class IIb
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Ireland
Manufacturer details
- EUDAMED SRN
- US-MF-000038968
- Authorised representative
- AMO Ireland IE-AR-000013513
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