ZCT7000230
by Johnson & Johnson Surgical Vision, Inc.
Ref ZCT7000230, ZCT7000240, ZCT4000320, ZCT3000230, ZCT7000220, ZCT3000290, ZCT7000130, ZCT7000270, ZCT7000280, ZCT8000230, ZCT7000210, ZCT4000230, ZCT7000320, ZCT7000260, ZCT3000330Model ZCT700, ZCT400, ZCT300, ZCT800
ZCT7000230 is a Class IIb device made by Johnson & Johnson Surgical Vision, Inc., registered in EUDAMED on 4 Mar 2026 (Basic UDI-DI B-USMF0000389680009146Y), 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-USMF0000389680009146Y | Date4 Mar 2026 | StatusActive |
Official records
- EUDAMED public site B-USMF0000389680009146Y
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Model / reference
- ZCT700, ZCT7000230, ZCT7000240, ZCT400, ZCT4000320, ZCT300, ZCT3000230, ZCT7000220, ZCT3000290, ZCT7000130, ZCT7000270, ZCT7000280, ZCT800, ZCT8000230, ZCT7000210, ZCT4000230, ZCT7000320, ZCT7000260, ZCT3000330
- Primary DI / UDI-DI
- D-USMF0000389680009146Y, D-USMF00003896800091674, D-USMF0000389680010505W, D-USMF0000389680006196T, D-USMF0000389680009126U, D-USMF0000389680006316H, D-USMF0000389680008947K, D-USMF0000389680009226X, D-USMF00003896800092473, D-USMF0000389680009737G, D-USMF0000389680009106Q, D-USMF0000389680010325U, D-USMF00003896800093272, D-USMF0000389680009206T, D-USMF0000389680006396Z
- Basic UDI-DI
- B-USMF0000389680009146Y, B-USMF00003896800091674, B-USMF0000389680010505W, B-USMF0000389680006196T, B-USMF0000389680009126U, B-USMF0000389680006316H, B-USMF0000389680008947K, B-USMF0000389680009226X, B-USMF00003896800092473, B-USMF0000389680009737G, B-USMF0000389680009106Q, B-USMF0000389680010325U, B-USMF00003896800093272, B-USMF0000389680009206T, B-USMF0000389680006396Z
- 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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