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MyLabClass C Advanced

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 101620020Model 6200

by Esaote S.p.A.

Identity

Trade Name
MyLabClass C Advanced EUDAMEDFDA UDI
Generic Name
General-purpose ultrasound imaging system FDA UDI
Model / Reference
6200 EUDAMED
101620020 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08056304450302 EUDAMEDFDA UDI
Basic UDI-DI
B-08056304450302 EUDAMED
FDA Product Code
IYO FDA UDI
ITX FDA UDI
IYN FDA UDI
EMDN Code
Z11040104 MULTIDISCIPLINARY ULTRASOUND SCANNERS (INTERNAL AND CARDIOLOGY, ETC.) EUDAMED
GMDN Term
General-purpose ultrasound imaging system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
892.1570 FDA UDI
892.1550 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

MyLabClass C Advanced 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 445398c0-7938-4f31-8be5-6ca0c0fce5d6 61 fields · synced Aug 3, 2026
  • FDA UDI 3a32d9d3-217f-48c0-a541-a187b2f95af8 32 fields · synced May 30, 2026