← Back to catalogue

Lacrivera

EUDAMED

Class IIb (EU MDR)

Ref VFF-5002

by Stephens Instruments

Identity

Trade Name
Lacrivera EUDAMED
Device Name
VERAPLUG FLEXFIT-STERILE PRE LOADED MEDIUM EUDAMED
Model / Reference
VFF-5002 EUDAMED

Identifiers

Primary DI / UDI-DI
00810799030030 EUDAMED
Basic UDI-DI
B-00810799030030 EUDAMED
EMDN Code
Q020703 LACRIMAL DUCT PLUGS 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

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

Category: Lacrimal punctum plug

Lacrivera by Stephens Instruments, Inc — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Lacrimal punctum plug.

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-000030661
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED b462a384-d799-4078-a4e5-68a78d2dc2d8 61 fields · synced Jul 27, 2026