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Zct8000170

EUDAMED

Class IIb (EU MDR)

Ref ZCT8000170Model ZCT800

by Johnson & Johnson Surgical Vision, Inc.

Identity

Model / Reference
ZCT800 EUDAMED
ZCT8000170 EUDAMED

Identifiers

Primary DI / UDI-DI
D-USMF00003896800096179 EUDAMED
Basic UDI-DI
B-USMF00003896800096179 EUDAMED
EMDN Code
P030102090301 IOLs, APHAKIC, MONOFOCAL, 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

Zct8000170 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

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Manufacturer

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

Sources (1)

  • EUDAMED 84e05f8a-06a6-48c0-a38b-47cb3804e0f7 61 fields · synced Jun 18, 2026