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Jaws insert, 5 x 330, Roeder HICURA

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref WA69382M

by Olympus Winter & Ibe GmbH

Identity

Trade Name
Jaws insert, 5 x 330, Roeder HICURA EUDAMED
Olympus FDA UDI
Generic Name
Suture knot pusher, reusable FDA UDI
Device Name
Hicura Accessories EUDAMED
Jaws insert "HICURA", 5 x 330, Roeder FDA UDI
Model / Reference
WA69382M EUDAMEDFDA UDI
Description
Jaws insert "HICURA", 5 x 330, Roeder FDA UDI

Identifiers

Catalog Number
WA69382M FDA UDI
Primary DI / UDI-DI
04042761079884 EUDAMEDFDA UDI
Basic UDI-DI
4042761111004H EUDAMED
Direct Marketing DI
04042761079884 EUDAMED
510(k) Number
K140624 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
L1899 ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Suture knot pusher, 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

Category: Electrical-only medical device connection cable, reusable

Jaws insert, 5 x 330, Roeder HICURA by Olympus Winter & Ibe GmbH — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

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 ab6e5a56-0d41-4751-8e49-4df38171ec77 61 fields · synced Oct 5, 2026
  • FDA UDI 1f2f1829-32f5-4beb-a2c6-113c90f66b4b 36 fields · synced May 30, 2026
  • EUDAMED 90e8d44f-97ca-4565-83b0-f8846b1b03f5 61 fields · synced Oct 5, 2026