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Sutter

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 370130P

by Sutter Medizintechnik GmbH

Identity

Trade Name
Sutter FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
Cables, Pencils and Adaptors EUDAMED
Bipolar cable 4.5m, 2x2.5mm pins for Ethicon Powerstar generators: for Erbe (except: ICC FDA UDI
Model / Reference
370130P EUDAMEDFDA UDI
Description
Bipolar cable 4.5m, 2x2.5mm pins for Ethicon Powerstar generators: for Erbe (except: ICC FDA UDI

Identifiers

Catalog Number
370130P FDA UDI
Primary DI / UDI-DI
ESUM370130P0 EUDAMEDFDA UDI
Basic UDI-DI
++ESUMTD08370000EK EUDAMED
Direct Marketing DI
ESUM370130P0 EUDAMED
FDA Product Code
GEI FDA UDI
EMDN Code
Z12010980 ELECTROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrical-only medical device connection cable, reusable

Sutter by Sutter Medizintechnik GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI b6684d8e-fbf1-4172-8f41-809d3f8ab312 35 fields · synced Jul 29, 2026
  • EUDAMED c719e1d0-73fe-4a2d-b74e-f84ec9ea3fc3 61 fields · synced Jul 29, 2026