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AutoProtect

EUDAMED

Class IIa (EU MDR)

Ref 9339Model type 820

by HTL-Strefa S.A.

Identity

Trade Name
AutoProtect EUDAMED
Device Name
Safety pen needle EUDAMED
Model / Reference
type 820 EUDAMED
9339 EUDAMED

Identifiers

Primary DI / UDI-DI
05903999608002 EUDAMED
Basic UDI-DI
590799609820MU EUDAMED
EMDN Code
A0101010201 HYPODERMIC PEN NEEDLES, WITH SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

AutoProtect by Htl Strefa S A — Class IIa — 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
HTL-Strefa S.A.
EUDAMED SRN
PL-MF-000002198

Sources (1)

  • EUDAMED 7c489872-3def-41d6-b4aa-acc40bdf200d 61 fields · synced Jun 19, 2026