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Burrer a

EUDAMED

Class I (EU MDR)

Ref 101Model Burrer

by Aktina Medical Corp

Identity

Device Name
Burrer a EUDAMED
Model / Reference
Burrer EUDAMED
101 EUDAMED

Identifiers

Primary DI / UDI-DI
05051659000090 EUDAMED
Basic UDI-DI
B-05051659000090 EUDAMED
EMDN Code
A0101010101 HYPODERMIC SYRINGE NEEDLES, WITH SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

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

Category: Hypodermic needle, single-use

Burrer a by Aktina Medical Corp — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hypodermic needle, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Aktina Medical Corp
EUDAMED SRN
US-MF-000005935
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED 021e8a30-2162-4e2f-8e18-9b6dec560347 61 fields · synced Oct 7, 2026