← Back to catalogue

Closed FLL white cap in blister packaging

EUDAMED

Class IIa (EU MDR)

Ref 06503300-SModel 06503300/S

by Elcam Medical Italy SpA

Identity

Trade Name
Closed FLL white cap in blister packaging EUDAMED
Device Name
Closed FLL white cap in blister packaging EUDAMED
Model / Reference
06503300/S EUDAMED
06503300-S EUDAMED

Identifiers

Primary DI / UDI-DI
08053323800101 EUDAMED
Basic UDI-DI
B-08053323800101 EUDAMED
EMDN Code
A070501 CAPS OR OBTURATORS, NON-PERFORABLE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Closed FLL white cap in blister packaging by Elcam Medical Italy Spa — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

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
IT-MF-000012119

Sources (1)

  • EUDAMED dda04c4a-b083-41a3-8ab8-39977258c4a8 61 fields · synced Jun 19, 2026