← Back to catalogue

Zxt300i310

EUDAMED

Class IIb (EU MDR)

Ref ZXT300I310Model ZXT300

by Johnson & Johnson Surgical Vision, Inc.

Identity

Model / Reference
ZXT300 EUDAMED
ZXT300I310 EUDAMED

Identifiers

Primary DI / UDI-DI
D-USMF0000389680017567D EUDAMED
Basic UDI-DI
B-USMF0000389680017567D EUDAMED
EMDN Code
P030102100301 IOLs, APHAKIC, MULTIFOCAL, TORIC, HYDROPHOBIC ACRYLIC EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Zxt300i310 by Johnson & Johnson Surgical Vision, Inc. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000038968
Authorised Representative
AMO Ireland IE-AR-000013513

Sources (1)

  • EUDAMED 8e62afc7-7b35-433b-a2b9-1663f546b98f 61 fields · synced Jun 19, 2026