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Jaws insert, 5 x 250, claw type, monopolar HICURA

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref WA69344S

by Olympus Winter & Ibe GmbH

Identity

Trade Name
Jaws insert, 5 x 250, claw type, monopolar HICURA EUDAMED
Olympus FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
Hicura Forceps - monopolar EUDAMED
Jaws insert "HICURA", 5 x 250, claw type, monopolar FDA UDI
Model / Reference
WA69344S EUDAMEDFDA UDI
Description
Jaws insert "HICURA", 5 x 250, claw type, monopolar FDA UDI

Identifiers

Catalog Number
WA69344S FDA UDI
Primary DI / UDI-DI
04042761079587 EUDAMEDFDA UDI
Basic UDI-DI
4042761110595D EUDAMED
Direct Marketing DI
04042761079587 EUDAMED
510(k) Number
K140624 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
L180402 ENDOSCOPIC ELECTROSURGERY FORCEPS, REUSABLE EUDAMED
GMDN Term
Rigid endoscopic tissue manipulation forceps, 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

Jaws insert, 5 x 250, claw type, monopolar HICURA by Olympus Winter & Ibe GmbH — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
DE-MF-000006729

Sources (3)

  • EUDAMED 90d58347-58b8-4aec-a9ec-cd08b4b8f612 61 fields · synced Jul 22, 2026
  • FDA UDI 015ab8a4-b60a-43c3-ae5d-801a3f226cb0 36 fields · synced May 30, 2026
  • EUDAMED 79026c2f-b5e5-4484-ab9e-d8fda2e176c7 61 fields · synced Jul 22, 2026