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Splinter Forcep Stieglitz

EUDAMED

Class I (EU MDR)

Ref 591

by Prilanta Surgical

Identity

Trade Name
Splinter Forcep Stieglitz EUDAMED
Device Name
Splinter Forcep Stieglitz EUDAMED
Model / Reference
591 EUDAMED

Identifiers

Primary DI / UDI-DI
G5485910 EUDAMED
Basic UDI-DI
++G548591NQ EUDAMED
EMDN Code
L031303 SWAB FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Splinter Forcep Stieglitz by Prilanta Surgical — Class I — 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
Prilanta Surgical
EUDAMED SRN
PK-MF-000038228
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED d854303b-9792-4d49-832c-39111c951e5d 61 fields · synced Jun 18, 2026