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Haemofine

EUDAMED

Class IIa (EU MDR)

Ref 8003Model type 810

by HTL-Strefa S.A.

Identity

Trade Name
Haemofine EUDAMED
Device Name
pen needle EUDAMED
Model / Reference
type 810 EUDAMED
8003 EUDAMED

Identifiers

Primary DI / UDI-DI
05907506237785 EUDAMED
Basic UDI-DI
B-05907506237785 EUDAMED
EMDN Code
A0101010202 HYPODERMIC PEN NEEDLES, W/O SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Haemofine by Htl Strefa S A — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
HTL-Strefa S.A.
EUDAMED SRN
PL-MF-000002198

Sources (1)

  • EUDAMED ad815308-5e19-4ccb-8ed9-aa92ee5cfb2b 61 fields · synced Jun 20, 2026