Trillium™

Trillium BIO Probe DP38T Adult 3/8 10PK

Registry build 21.09.26
2manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

All of them in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code DPT
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
RWD Life Science Co., Ltd. Shenzhen Guangdong Manufacturer 4

Record

Regulatory record for Trillium™
Listed by Medtronic, Inc., United States
FDA product code DPT
Device type Probe, Blood-Flow, Extravascular
Device class Class 2
Regulation 21 CFR 870.2120
Establishment Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K132730
Record published 2017-01-03
Record revised 2018-12-13 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number
Storage Storage environment temperature up to 50 °C
Packaging Pack of 10
Distribution end date 2018-10-05

Catalogue Numbers

Catalogue numbers for Trillium™
Catalogue number Size Status
DP38PT 6.35 MM Port Outer Diameter Withdrawn
DP38T 9.53 MM Port Outer Diameter Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Medex ICU Medical, Inc 138
Bio-Probe™ Medtronic, Inc. 21
Probe, Blood-Flow, Extravascular Medtronic, Inc. 10
Moor Instruments Ltd Moor Instruments Ltd. 3
Trillium™ Bio-Probe® Medtronic, Inc. 2
FloProbe 3/8’’ x 3/8” (Non Sterile) Movair, Inc. 1
FloProbe 1/4’’ x 1/4″ (Non Sterile) Movair, Inc. 1
FloProbe 1/4’’ x 1/4’’ (Sterile) Movair, Inc. 1
I2P24 Doppler Probe Deltex Medical Limited 1
I2S6 Doppler Probe Deltex Medical Limited 1
moorFLPI-2 Review PC Software Moor Instruments Ltd. 1
moorFLPI2- Measurement PC Software Moor Instruments Ltd. 1

Showing 12 of 17. All products under Probe, Blood-Flow, Extravascular

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K132730 2014-05-30
K133903 2014-04-10

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