Ust-5419
Ust-5419 is a Class II device made by Fujifilm Corporation, listed in FDA GUDID since 18 Jul 2021 (UDI-DI 04573596212806), registry data as of 1 Jun 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04573596212806 | Date18 Jul 2021 | StatusListed |
Official records
- AccessGUDID record 04573596212806
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Extracorporeal ultrasound imaging transducer, hand-held
- Model / reference
- UST-5419
- Primary DI / UDI-DI
- 04573596212806
- FDA product code
- IYO, IYN, ITX
- GMDN term
- Extracorporeal ultrasound imaging transducer, hand-held
- Device class
- Class II
- Regulation number
- 892.1560, 892.1550, 892.1570
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Extracorporeal ultrasound imaging transducer, hand-held.
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- GP-C01 99-7903-00 by Interson Corporation
- L4-20t-D 5874154 by GE Medical Systems CO. Ltd
- C10-3 P31043-02 by Fujifilm Sonosite, Inc.
- Ultrasound Probes 7L4 by Beijing iTrason Technologies Co., Ltd.
- L19-5 P31040-02 by Fujifilm Sonosite, Inc.
- 8V3 Transducer 11014578 by SIEMENS MEDICAL SOLUTIONS USA, INC.
- 5V1 Transducer 11291796 by SIEMENS MEDICAL SOLUTIONS USA, INC.
- C1-5-D H40452LE by GE Healthcare Japan Corporation
- 2D Abdominal Probe K2DAB00 by KOELIS