Identity
- Trade Name
- MasterVu B EUDAMEDMaster-Vu B-Scan Ophthalmic Ultrasound System FDA UDI
- Generic Name
- Ophthalmic ultrasound imaging system FDA UDI
- Device Name
- MasterVu B-Scan EUDAMEDThe Master-Vu B-Scan Ophthalmic Ultrasound System is a non-invasive, active, diagnostic and biometric device intended for use in ophthalmic applications by imaging the internal structures of the eye. They system consists of a sealed, posterior segment B-probe and cable designed to interface with any standard personal computer (host PC). The probe utilizes a 12 MHz transducer with a sector scanning probe operating on the host PC. The software for the Master-Vu B-Scan allows the host PC to function as the main control interface and display for the B-scan system. The system is provided with the portable, hand-held B-probe with 12 MHz transducer, USB cable, Master-Vu B software on a flash drive, carry case and user manual. FDA UDI
- Model / Reference
- MV5600 EUDAMEDFDA UDI
- Description
- The Master-Vu B-Scan Ophthalmic Ultrasound System is a non-invasive, active, diagnostic and biometric device intended for use in ophthalmic applications by imaging the internal structures of the eye. They system consists of a sealed, posterior segment B-probe and cable designed to interface with any standard personal computer (host PC). The probe utilizes a 12 MHz transducer with a sector scanning probe operating on the host PC. The software for the Master-Vu B-Scan allows the host PC to function as the main control interface and display for the B-scan system. The system is provided with the portable, hand-held B-probe with 12 MHz transducer, USB cable, Master-Vu B software on a flash drive, carry case and user manual. FDA UDI
Identifiers
- Catalog Number
- MV5600 FDA UDI
- Primary DI / UDI-DI
- 00896100002118 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00896100002118 EUDAMED
- 510(k) Number
- K073196 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
- Poland 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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MasterVu B by Sonomed, Inc. — 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00896100002118 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Sonomed, Inc.
- EUDAMED SRN
- US-MF-000002342
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED fb6a5b76-36c0-403b-a98c-c0de30d9e030 61 fields · synced Jun 19, 2026
- FDA UDI 38058179-a8e7-46cc-a40d-5a3fadd51993 36 fields · synced May 30, 2026