FUJIFILM
- Primary DI
- 00860007188367
- Brand
- FUJIFILM
- Company
- Fujifilm Healthcare Americas Corporation
- Model
- CC13HPB5
- Device description
- The CC13HPB5 probe is an intraoperative ultrasound transducer with dual curved array. This transducer can be used for intraoperative ultrasound imaging. The CC13HPB5 probe is intended for use by trained personnel (doctors, sonographers, and so on) for diagnostic ultrasound evaluation during intraoperative procedures. This device is not indicated for ophthalmic applications.
- Published
- 2026-09-29
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes#
Product Code Classifications#
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K191233 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00860007188367 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00860007188367 | 00860007188367 | 860007188367 | 0860007188367 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical ultrasound imaging transducer | A hand-held ultrasound imaging transducer assembly designed to be positioned within a surgical site for localized intraoperative imaging applications. It is sometimes referred to as a surgical probe or fingertip probe. It steers, focuses, and detects the ultrasound beam and resulting echoes either mechanically or electronically. This group of devices includes ultrasound imaging transducer assemblies used with A-mode, B-mode, M-mode, Doppler, colour Doppler (CD), and duplex (combination imaging, Doppler and/or colour flow) scanning capabilities. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Hydrogen Peroxide |
Regulatory Flags#
- DUNS number
- 041767039
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- true
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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|---|---|---|---|---|
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| 00869047000431 | Synapse Select | 4.X.X | 2018-09-27 | |
| 00860007188305 | C9150LA | C9150LA | 2021-07-01 | |
| 00854904006015 | Synapse CardioVascular | Synapse Cardiology PACS Software License | 2016-09-23 | |
| 00860014745003 | FUJIFILM Stiffening Wire (SW-2000) | SW-2000 | 2025-12-18 | |
| 00854904006039 | Synapse Pathology | Synapse Pathology Software License | 2023-06-16 | |
| 00860007188343 | Transducer S12BP4 | S12BP4 | 2022-06-08 | |
| 00854904006060 | Synapse Enterprise Viewer | Synapse Enterprise Viewer | 2019-05-23 | |
| 00854904006022 | Synapse MPR Fusion | Synapse MPR Fusion Software License | 2016-09-23 | |
| 00854904006053 | Synapse Mobility | Synapse Mobility Base Package | 2016-09-29 | |
| 00860007188312 | UST 5550-R | UST 5550-R | 2021-07-01 | |
| 00860007188329 | UST-9150 | UST-9150 | 2021-07-01 | |
| 00860007188336 | UST-52114P-B | UST-52114P-B | 2021-07-01 | |
| 00869047000455 | D&K Technologies | DK-ARM-KIT | 2021-02-15 | |
| 00869047000462 | D&K Technologies | DK-STAND-KIT | 2021-02-15 | |
| 00869047000448 | HITACHI HEALTHCARE AMERICAS | C9150LA | 2020-06-29 | |
| 00869047000400 | HITACHI HEALTHCARE AMERICAS | UST-5550-R | 2018-07-23 | |
| 00869047000417 | HITACHI HEALTHCARE AMERICAS | UST-9150 | 2018-07-23 | |
| 00869047000424 | HITACHI HEALTHCARE AMERICAS | UST-52114P-B | 2018-07-23 |
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| 00198953172551 | Vivid | GE Vingmed Ultrasound A/S | IYO | 2026-09-21 |
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