Dunelee Sentinelle

VT 3T 8CH TT TITAN FULL SET w GRID contains one box of 10 Biopsy grids, one Interface box, one Medial array, one Lateral array left and right, one Single loop left and right, one Medial…

Registry build 21.09.26

VT 3T 8CH TT TITAN FULL SET w GRID contains one box of 10 Biopsy grids, one Interface box, one Medial array, one Lateral array left and right, one Single loop left and right, one Medial plug and one Patient support

9manufacturers in China registered for this device type
1catalogue number
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (3), Guangdong (2), Tianjin (2).

Chinese manufacturers registered for FDA product code MOS
Manufacturer City Province Registered as Device types
GE Healthcare (China) Co., Ltd. Beijing Beijing Specification developer 22
Shanghai United Imaging Healthcare Co., Ltd. Shanghai Shanghai Manufacturer 12
Siemens Shenzhen Magnetic Resonance Ltd. Shenzhen Guangdong Contract manufacturer 8
Philips Healthcare (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
GE Healthcare (Tianjin) Company Limited Tianjin Tianjin Specification developer 5
GE Healthcare (China) Co., Ltd. – Tianjin Tianjin Tianjin Specification developer 3
Shenzhen RF Tech Co., Ltd. Shenzhen Guangdong Complaint-file establishment 2
Shanghai Chenguang Medical Technologies Co., Ltd. Shanghai Shanghai Contract manufacturer 2
Shanghai Chenshi Medical Instruments Co., Ltd. Shanghai Shanghai Exporter 2

Record

Regulatory record for Dunelee Sentinelle
Listed by Philips Medical Systems Nederland B.V., Netherlands
FDA product code MOS
Device type Coil, Magnetic Resonance, Specialty
Device class Class 2
Regulation 21 CFR 892.1000
Establishment Contract manufacturer, Remanufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2023-05-23
Record revised 2023-09-26 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries expiry date, serial number
Storage Storage environment atmospheric pressure 15 to 30 °C; Storage environment humidity 30 to 75 % RH

Catalogue Numbers

Catalogue numbers for Dunelee Sentinelle
Catalogue number Size Status
989603216941 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Dunlee Sentinelle Philips Medical Systems Nederland B.V. 192
Invivo Philips DS North America LLC 185
Philips Philips DS North America LLC 88
Coil, Magnetic Resonance, Specialty Usa Instruments, Inc. 50
Philips Shanghai Chenguang Medical Technologies Co., Ltd. 50
GE Philips DS North America LLC 41
MR Coils Philips Medical Systems Nederland B.V. 37
MRI Coils Philips DS North America LLC 24
DuoFLEX® Coil Suite M R Instruments, Inc. 20
RFT Shenzhen RF Tech Co., Ltd. 18
AtamA™ System Monteris Medical Corp 17
Philips Sentinelle Philips Medical Systems Nederland B.V. 16

Showing 12 of 713. All products under Coil, Magnetic Resonance, Specialty

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K262330 2026-07-30
K262294 2026-07-24
K254190 2026-01-14
K243033 2024-10-18
K242879 2024-10-18
K242096 2024-08-12

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer