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Tee022

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 9600170000

by Esaote S.p.A.

Identity

Trade Name
TEE022 EUDAMED
TEE FDA UDI
Generic Name
Oesophageal ultrasound imaging transducer, reusable FDA UDI
Device Name
TEE022 EUDAMED
Probe TEE022 complete name FDA UDI
Model / Reference
9600170000 EUDAMEDFDA UDI
Description
Probe TEE022 complete name FDA UDI

Identifiers

Primary DI / UDI-DI
08056304452047 EUDAMEDFDA UDI
Basic UDI-DI
B-08056304452047 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

Tee022 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 62476237-f632-4ed4-bc32-44ac55becae2 61 fields · synced Jun 18, 2026
  • FDA UDI f91d5bd9-dce9-46ed-914e-39855de17b5a 33 fields · synced May 25, 2026