← Back to catalogue

Shaft, 5 x 250, monopolar HICURA

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref WA69300S

by Olympus Winter & Ibe GmbH

Identity

Trade Name
Shaft, 5 x 250, monopolar HICURA EUDAMED
Olympus FDA UDI
Generic Name
Orthopaedic implantation sleeve, reusable FDA UDI
Device Name
Hicura Shaft - monopolar EUDAMED
Shaft "HICURA", 5 x 250, monopolar FDA UDI
Model / Reference
WA69300S EUDAMEDFDA UDI
Description
Shaft "HICURA", 5 x 250, monopolar FDA UDI

Identifiers

Catalog Number
WA69300S FDA UDI
Primary DI / UDI-DI
04042761079129 EUDAMEDFDA UDI
Basic UDI-DI
40427611106558 EUDAMED
Direct Marketing DI
04042761079129 EUDAMED
510(k) Number
K140624 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
L180302 ENDOSCOPIC ELECTROSURGERY HANDPIECES, REUSABLE EUDAMED
GMDN Term
Orthopaedic implantation sleeve, reusable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Shaft, 5 x 250, monopolar HICURA by Olympus Winter & Ibe GmbH — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000006729

Sources (3)

  • EUDAMED d5cd1fc7-d45a-4237-a061-4799116284e8 61 fields · synced Jun 19, 2026
  • FDA UDI ecb7ad13-c49f-45c0-b810-9f1709960eba 36 fields · synced May 29, 2026
  • EUDAMED 36278efc-142d-4c38-82c6-38031c127b16 61 fields · synced Jun 19, 2026