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Gimmi

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref T.9539.08

by Gimmi GmbH

Identity

Trade Name
Gimmi FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
HF Cable, Handle, Adapter EUDAMED
MONOPOLAR CABLE, Ø 4 MM PLUG INSTRUMENT UNIT SIDE Ø 8 MM TYPE BOVIE LENGTH 500 CM FDA UDI
Model / Reference
T.9539.08 EUDAMEDFDA UDI
Description
MONOPOLAR CABLE, Ø 4 MM PLUG INSTRUMENT UNIT SIDE Ø 8 MM TYPE BOVIE LENGTH 500 CM FDA UDI

Identifiers

Catalog Number
T.9539.08 FDA UDI
Primary DI / UDI-DI
04049047108375 EUDAMEDFDA UDI
Basic UDI-DI
4049047LEJ04ADA27DRBFG EUDAMED
Direct Marketing DI
04049047108375 EUDAMED
FDA Product Code
IKD 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
890.1175 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

Yes

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

Gimmi by Gimmi 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

Manufacturer
Gimmi GmbH

Sources (2)

  • FDA UDI cb87ef11-0f2d-4017-9c24-e1b2a744f6c4 35 fields · synced Jun 19, 2026
  • EUDAMED 71d959e7-4596-4e86-94fe-2a812ddbca92 61 fields · synced Jun 19, 2026