← Back to catalogue

Jaws insert, 5 x 250, Maryland, monopolar HICURA

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref WA69350SRef WA69358S

by Olympus Winter & Ibe GmbH

Identity

Trade Name
Jaws insert, 5 x 250, Maryland, monopolar HICURA EUDAMED
Jaws insert, 5 x 250, Maryland 90° angled, monopolar HICURA EUDAMED
Olympus FDA UDI
Generic Name
Dissection forceps FDA UDI
Device Name
Hicura Forceps - monopolar EUDAMED
Model / Reference
WA69350S EUDAMEDFDA UDI
WA69358S EUDAMEDFDA UDI

Identifiers

Catalog Number
WA69350S FDA UDI
WA69358S FDA UDI
Primary DI / UDI-DI
04042761079648 EUDAMEDFDA UDI
04042761079747 EUDAMEDFDA UDI
Basic UDI-DI
4042761110595D EUDAMED
Direct Marketing DI
04042761079648 EUDAMED
04042761079747 EUDAMED
510(k) Number
K140624 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
L180402 ENDOSCOPIC ELECTROSURGERY FORCEPS, REUSABLE EUDAMED
GMDN Term
Dissection forceps 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, Maryland, 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

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

Manufacturer

EUDAMED SRN
DE-MF-000006729

Sources (6)

  • EUDAMED 64c15c91-8528-450c-adf2-bf0260151eeb 61 fields · synced Jul 9, 2026
  • EUDAMED 84a9f10d-d05f-4938-b382-518dfe0ac183 61 fields · synced May 18, 2026
  • FDA UDI 6cfbee4e-bf74-4758-8d9a-837dc3f2e0de 34 fields · synced May 29, 2026
  • FDA UDI 11dc157d-2dd2-4281-ba10-08df08f2e530 34 fields · synced May 30, 2026
  • EUDAMED 33b59f42-0d62-4854-a4c0-adbfc7058b08 61 fields · synced Jun 19, 2026
  • EUDAMED 3d7a079b-dcf9-4e4f-8a3a-78cee7502e84 61 fields · synced Jul 9, 2026