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Intermediate Cable

FDA UDI

Class II (US FDA UDI)

by Italian Engineering Srl

Identity

Trade Name
INTERMEDIATE CABLE FDA UDI
Generic Name
Electrosurgical cable adaptor FDA UDI
Device Name
To be used with ATTIVA device (K220505). FDA UDI
Model / Reference
CBEL-R-IE FDA UDI
Description
To be used with ATTIVA device (K220505). FDA UDI

Identifiers

Primary DI / UDI-DI
05060224334072 FDA UDI
510(k) Number
K220505 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical cable adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 200 Millimeter FDA UDI

Category: Electrosurgical cable adaptor

Intermediate Cable by Italian Engineering Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical cable adaptor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4b54d4bc-91d9-4f53-9c5c-1f1b0cd40d11 35 fields · synced May 30, 2026