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Logiq
FDA UDIEUDAMEDClass II (US FDA UDI)
Ref LOGIQ E10s R2R3 to R4 SW Upgrade W / 5946723Model LOGIQ E10s
Identity
- Trade Name
- LOGIQ FDA UDI
- Generic Name
- General-purpose ultrasound imaging system FDA UDI
- Device Name
- LOGIQ E10s EUDAMEDLOGIQ E10s R2/R3 to R4 SW Upgrade including Wireless FDA UDI
- Model / Reference
- LOGIQ E10s EUDAMEDLOGIQ E10s R2R3 to R4 SW Upgrade W / 5946723 EUDAMEDE10s R2R3 to R4 SW Upgrade W FDA UDI
- Description
- LOGIQ E10s R2/R3 to R4 SW Upgrade including Wireless FDA UDI
Identifiers
- Catalog Number
- 5946723 FDA UDI
- Primary DI / UDI-DI
- 00195278835772 EUDAMEDFDA UDI
- Basic UDI-DI
- 8406821BUG00033GT EUDAMED
- 510(k) Number
- K231989 FDA UDI
- FDA Product Code
- IYN FDA UDIITX FDA UDIIYO FDA UDI
- EMDN Code
- Z11040101 INTERNAL ULTRASOUND SCANNERS EUDAMED
- GMDN Term
- General-purpose ultrasound imaging system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1550 FDA UDI892.1570 FDA UDI892.1560 FDA UDI
- Market of Registration
- Austria 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
Yes
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
MR Unsafe FDA UDI
Logiq by GE Ultrasound Korea Ltd. — Class II — FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Cleared under the same submission
K231989 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- GE Ultrasound Korea Ltd.
Sources (2)
- FDA UDI a163b1cb-165b-4067-b2bd-9f7cdd13d718 36 fields · synced Oct 6, 2026
- EUDAMED f8aa76e4-30f5-457a-9741-aa810a4767c3 61 fields · synced Jul 15, 2026