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St2612

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 121200801

by Esaote S.p.A.

Identity

Trade Name
ST2612 EUDAMEDFDA UDI
Generic Name
Oesophageal ultrasound imaging transducer, reusable FDA UDI
Device Name
ST2612 EUDAMED
Model / Reference
121200801 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08056304451576 EUDAMEDFDA UDI
Basic UDI-DI
B-08056304451576 EUDAMED
FDA Product Code
ITX FDA UDI
EMDN Code
Z1104020301 TRANSESOPHAGEAL ULTRASOUND PROBES, TWO–DIMENSIONAL EUDAMED
GMDN Term
Oesophageal ultrasound imaging transducer, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1570 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

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Hydrogen Peroxide FDA UDI

St2612 by Esaote S.p.A. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Esaote S.p.A.
EUDAMED SRN
IT-MF-000019024

Sources (2)

  • EUDAMED 4c48702a-a122-42bc-87cb-ce61024bd223 61 fields · synced Jun 20, 2026
  • FDA UDI 29941b26-1131-49f3-8f7d-693c5d02d93b 32 fields · synced May 30, 2026