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Ppt Heligon 6b

EUDAMED

Class IIa (EU MDR)

Ref PPT103

by Bausch & Lomb GmbH

Identity

Trade Name
PPT HELIGON 6B EUDAMED
Device Name
Cataract Per Procedure Tray EUDAMED
Model / Reference
PPT103 EUDAMED

Identifiers

Primary DI / UDI-DI
24058935006703 EUDAMED
Basic UDI-DI
B-24058935006703 EUDAMED
EMDN Code
Q021199 OPHTHALMIC SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Ppt Heligon 6b by Bausch & Lomb GmbH — Class IIa — 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

Manufacturer
Bausch & Lomb GmbH
EUDAMED SRN
DE-MF-000009142

Sources (1)

  • EUDAMED bb2a803a-3594-4911-af12-119702efd134 61 fields · synced Jun 18, 2026