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Reusable Bipolar Cords

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 10-6011

by Kirwan Surgical Products LLC

Identity

Trade Name
Kirwan FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Reusable Bipolar Cords EUDAMED
Reusable Bipolar Silicone Cord 12 ft. (3.6m) with Lemo Plug (for Storz-Type Premier) FDA UDI
Model / Reference
10-6011 EUDAMEDFDA UDI
Description
Reusable Bipolar Silicone Cord 12 ft. (3.6m) with Lemo Plug (for Storz-Type Premier) FDA UDI

Identifiers

Primary DI / UDI-DI
00841019102312 EUDAMEDFDA UDI
Basic UDI-DI
08410191RBC1032M EUDAMED
510(k) Number
K831236 FDA UDI
FDA Product Code
GEI FDA UDI
EMDN Code
L1899 ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I 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

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 12 Feet FDA UDI

Category: Electrical-only medical device connection cable, reusable

Reusable Bipolar Cords by Kirwan Surgical Products Llc — Class I — 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
US-MF-000008222
Authorised Representative
MPS Medical Product Service GmbH DE-AR-000005009

Sources (2)

  • EUDAMED 232f33d6-a86f-4c16-80ca-178ac671d1a5 61 fields · synced Jul 11, 2026
  • FDA UDI bbffe1df-1ca4-4b38-92d9-b5e557e233bc 36 fields · synced May 30, 2026