← Back to catalogue

E3190 Katzin-Barraquer Corneal Forceps

EUDAMED

Class I (EU MDR)

Ref E3190

by Bausch & Lomb GmbH

Identity

Trade Name
E3190 Katzin-Barraquer Corneal Forceps EUDAMED
Device Name
Reusable devices EUDAMED
Model / Reference
E3190 EUDAMED

Identifiers

Primary DI / UDI-DI
04058935010423 EUDAMED
Basic UDI-DI
4058935-000000-AC EUDAMED
Direct Marketing DI
04058935010423 EUDAMED
EMDN Code
L170299 OPHTHALMOLOGY FORCEPS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

E3190 Katzin-Barraquer Corneal Forceps by Bausch & Lomb GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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

Manufacturer

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

Sources (1)

  • EUDAMED 73450a2f-303b-46e9-8ba2-37334c8b6567 61 fields · synced Jun 20, 2026