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St-Adpt-30

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ST-ADPT-30Model SENSITHERM MULTI - Adapter cable

by FIAB S.p.A.

Identity

Trade Name
SENSITHERM MULTI FDA UDI
Generic Name
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
The ST-ADPT-30 adapter cable is an accessory for the SENSITHERM MULTI system that can be inserted in a dedicated socket on the handle of the ST-PTCBL patient cable for connecting the conductive terminals of ST -Probe to a mapping system. At one end, the adapter cable is equipped with a custom plug compatible with the dedicated port in the patient cable. The other end of the cable contains seven single pole polyurethane cables, each one ending in a 2mm touch-proof plug compatible with the input ports of a mapping system. FDA UDI
Model / Reference
SENSITHERM MULTI - Adapter cable EUDAMED
ST-ADPT-30 EUDAMEDFDA UDI
Description
The ST-ADPT-30 adapter cable is an accessory for the SENSITHERM MULTI system that can be inserted in a dedicated socket on the handle of the ST-PTCBL patient cable for connecting the conductive terminals of ST -Probe to a mapping system. At one end, the adapter cable is equipped with a custom plug compatible with the dedicated port in the patient cable. The other end of the cable contains seven single pole polyurethane cables, each one ending in a 2mm touch-proof plug compatible with the input ports of a mapping system. FDA UDI

Identifiers

Catalog Number
ST-ADPT-30 FDA UDI
Primary DI / UDI-DI
08058480754618 EUDAMEDFDA UDI
Basic UDI-DI
803300326103000001L3 EUDAMED
Direct Marketing DI
08058480754618 EUDAMED
510(k) Number
K192210 FDA UDI
FDA Product Code
IKD FDA UDI
EMDN Code
Z129080 VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - 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
890.1175 FDA UDI
Market of Registration
Italy 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

St-Adpt-30 by FIAB S.p.A. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
FIAB S.p.A.
EUDAMED SRN
IT-MF-000005988

Sources (2)

  • EUDAMED ff3eac47-b1e4-48f4-867f-151ee3a1ab55 61 fields · synced Jun 19, 2026
  • FDA UDI 0fb49c55-6836-4b48-b9d2-8c2ac2987bbc 37 fields · synced May 30, 2026