← Back to catalogue

Vivid iq

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref Vivid iq v206/5877072Model Vivid iq

by GE Medical Systems CO. Ltd

Identity

Trade Name
Vivid FDA UDI
Generic Name
Cardiovascular ultrasound imaging system FDA UDI
Device Name
Vivid iq EUDAMED
Vivid iq R6 basic console FDA UDI
Model / Reference
Vivid iq EUDAMED
Vivid iq v206/5877072 EUDAMED
iq v206 FDA UDI
Description
Vivid iq R6 basic console FDA UDI

Identifiers

Primary DI / UDI-DI
00195278421388 EUDAMEDFDA UDI
Basic UDI-DI
8406821BUG00254HD EUDAMED
Direct Marketing DI
00195278421388 EUDAMED
510(k) Number
K221148 FDA UDI
FDA Product Code
IYO FDA UDI
ITX FDA UDI
IYN FDA UDI
EMDN Code
Z11040102 CARDIOLOGY ULTRASOUND SCANNERS EUDAMED
GMDN Term
Cardiovascular 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
France 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

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

No

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
MRI Safety
MR Unsafe FDA UDI

Vivid iq by GE Medical Systems CO. Ltd — Class IIa — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000001856
Authorised Representative
GE Medical Systems SCS FR-AR-000000344

Sources (2)

  • EUDAMED 86007e82-49c4-4c93-9030-b569ced2c127 61 fields · synced Oct 6, 2026
  • FDA UDI 826ac022-8091-4fe5-9591-a6d0476b6e89 35 fields · synced May 30, 2026