Identity
- Trade Name
- MasterVu A EUDAMEDMaster-Vu A-Scan Ophthalmic Ultrasound System FDA UDI
- Generic Name
- Ophthalmic ultrasound imaging system FDA UDI
- Device Name
- MasterVu A-Scan EUDAMEDThe Master-Vu A-Scan Ophthalmic Ultrasound System is a non-invasive, active device intended for imaging ocular features for diagnostic purposes. The A-Scan system allows for measuring the axial length (AXL), anterior chamber depth, and lens thickness of an eye and for calculating the associated IOL power for an implanted lens. The Master-Vu A-Scan can be used to collect scan data using the direct contact or immersion method. There are five examination modes: Cataract, Dense Cataract, Aphakic, Pseudophakic and 4-Gate Manual. The Master-Vu A-Scan system includes the A-Scan console, a 10 MHz A-probe, foot switch, flash drive with A-scan software, USB cable, carry case and operator manual. FDA UDI
- Model / Reference
- MV4500 EUDAMEDFDA UDI
- Description
- The Master-Vu A-Scan Ophthalmic Ultrasound System is a non-invasive, active device intended for imaging ocular features for diagnostic purposes. The A-Scan system allows for measuring the axial length (AXL), anterior chamber depth, and lens thickness of an eye and for calculating the associated IOL power for an implanted lens. The Master-Vu A-Scan can be used to collect scan data using the direct contact or immersion method. There are five examination modes: Cataract, Dense Cataract, Aphakic, Pseudophakic and 4-Gate Manual. The Master-Vu A-Scan system includes the A-Scan console, a 10 MHz A-probe, foot switch, flash drive with A-scan software, USB cable, carry case and operator manual. FDA UDI
Identifiers
- Catalog Number
- MV4500 FDA UDI
- Primary DI / UDI-DI
- 00896100002101 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00896100002101 EUDAMED
- 510(k) Number
- K100252 FDA UDI
- FDA Product Code
- IYO FDA UDI
- EMDN Code
- Z11040199 ULTRASOUND SCANNERS - OTHER EUDAMED
- GMDN Term
- Ophthalmic ultrasound imaging system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1560 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
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MasterVu A by Sonomed, Inc. — Class IIa — FDA_510K, MDD — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K073196 | Class IIa | Active |
| EUDAMED | European Union | CE/MDD | B-00896100002101 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Sonomed, Inc.
- EUDAMED SRN
- US-MF-000002342
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (3)
- EUDAMED 0358ec0a-a4ff-4864-b2f5-111661f78140 61 fields · synced Jul 17, 2026
- FDA UDI ee66fb9e-a068-4ce3-95ff-37a9f2515c4a 36 fields · synced May 29, 2026
- FDA 510(k) K073196 1 fields · synced May 18, 2026