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E1796 Forceps Suture Castroviejo

EUDAMED

Class I (EU MDR)

Ref E1796

by Bausch & Lomb GmbH

Identity

Trade Name
E1796 Forceps Suture Castroviejo EUDAMED
Device Name
Reusable devices EUDAMED
Model / Reference
E1796 EUDAMED

Identifiers

Primary DI / UDI-DI
04058935013011 EUDAMED
Basic UDI-DI
4058935-000000-AC EUDAMED
Direct Marketing DI
04058935013011 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

E1796 Forceps Suture Castroviejo 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

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Manufacturer

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

Sources (1)

  • EUDAMED 6515c5cc-0304-4e34-94e2-e36c1bc1eba1 61 fields · synced Jun 17, 2026