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Skene Tenaculum Forceps, 23cm

EUDAMED

Class I (EU MDR)

Ref RAE-386-23R

by Rhein Enterprises (Pvt) Ltd

Identity

Trade Name
Skene Tenaculum Forceps, 23cm EUDAMED
Device Name
Reusable, Stainless Steel, Non-Sterile Surgical Forceps EUDAMED
Model / Reference
RAE-386-23R EUDAMED

Identifiers

Primary DI / UDI-DI
+G072RAE38623R0. EUDAMED
Basic UDI-DI
++G072RUFORCEPSSJ EUDAMED
Direct Marketing DI
+G072RAE38623R0. EUDAMED
EMDN Code
L03130401 TISSUE AND ORGAN GRASPING FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Skene Tenaculum Forceps, 23cm by Rhein Enterprises (Pvt) Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PK-MF-000036086
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED a4941772-fcf4-4e4e-ac65-318983c8bf19 61 fields · synced Jun 18, 2026