Torqr™

Cath 041002JM Torqr USA MKT 6FR W/O CE

Registry build 21.09.26
5manufacturers in China registered for this device type
32catalogue numbers in this listing
5510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (2), Tianjin (1), Shanghai (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DRF
Manufacturer City Province Registered as Device types
Jiangyin Sinbon Electronics Co Ltd Jiangyin Jiangsu Contract manufacturer 13
Palconn Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 2
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Tianjin Ethylene Oxide Sterilization Technology Co., Ltd. Tianjin Tianjin Contract manufacturer 4
Shanghai Microport EP Medtech Co., Ltd. Shanghai Shanghai Manufacturer 3

Record

Regulatory record for Torqr™
Listed by Medtronic, Inc., United States
FDA product code DRF
Device type Catheter, Electrode Recording, Or Probe, Electrode Recording
Device class Class 2
Regulation 21 CFR 870.1220
Establishment Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K190132
Record published 2020-07-23
Record revised 2023-10-09 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Storage Handling environment humidity up to 85 % RH; Handling environment temperature -31 to 140 °F; Special storage condition: Keep Dry; Storage environment temperature 59 to 86 °F
Distribution end date 2023-06-14

Catalogue Numbers

Catalogue numbers for Torqr™
Catalogue number Size Status
041865CS Catheter size 1.7mm (5 Fr) In distribution
041005DM Catheter size 2.0mm (6 Fr) In distribution
04122UM Usable length 110 cm In distribution
041005UM Electrode spacing 5 mm In distribution
041565CS Electrode spacing 2.5.2 mm In distribution
04125JM Usable length 110 cm In distribution
041010UM Electrode spacing 10 mm In distribution
04130DS Usable length 110 cm In distribution
041890CS Electrode spacing 2.8.2 mm In distribution
041002UM Usable length 110 cm In distribution
041005UM Catheter size 2.0mm (6 Fr) In distribution
041010UM Catheter size 2.0mm (6 Fr) In distribution
041005DM Usable length 110 cm In distribution
041002JM Catheter size 2.0mm (6 Fr) In distribution
04125UM Catheter size 1.7mm (5 Fr) In distribution
041005JM Usable length 110 cm In distribution
041010JM Electrode spacing 10.10.10 mm In distribution
04122JM Electrode spacing 2.5.2 mm In distribution
041590CS Catheter size 1.7mm (5 Fr) In distribution
041010JM Usable length 110 cm In distribution
04130DS Usable length 110 cm Withdrawn
041002JM Electrode spacing 2.5.2 mm Withdrawn
04122JM Electrode spacing 2.5.2 mm Withdrawn
041590CS Usable length 90 cm Withdrawn
04122UM Usable length 110 cm Withdrawn
041890CS Electrode spacing 2.8.2 mm Withdrawn
041865CS Electrode spacing 2.8.2 mm Withdrawn
041565CS Catheter size 1.7 mm (5 Fr) Withdrawn
041005JM Catheter size 2.0 mm (6 Fr) Withdrawn
041002UM Electrode spacing 2.5.2 mm Withdrawn
04125JM Usable length 110 cm Withdrawn
04125UM Electrode spacing 5 mm Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Map-iT Access Point Medical, LLC 420
Woven Boston Scientific Corporation 126
Inquiry™ Irvine Biomedical. Inc. 122
Webster Biosense Webster, Inc. 121
Viking™ Boston Scientific Corporation 81
EasyFinder Fixed Curve Diagnostic Catheter Shanghai Microport EP Medtech Co., Ltd. 56
Supreme™ St. Jude Medical Cardiovascular Division 55
Celsius Biosense Webster, Inc. 47
Response™ St. Jude Medical Cardiovascular Division 46
Catheter, Electrode Recording, Or Probe, Electrode Recording Medtronic, Inc. 27
Lasso NAV Biosense Webster, Inc. 22
AcQRate Dx Fixed Curve Catheter VascoMed GmbH 20

Showing 12 of 112. All products under Catheter, Electrode Recording, Or Probe, Electrode Recording

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K233397 2023-12-02
K190132 2019-07-30
K183547 2019-07-30
K162892 2016-11-15
K153139 2016-05-06

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2015-09-29 Class II Under Investigation by firm 64 units of Achieve Electrical Cables were shipped with a potential sterility breach. 64 units 2016-03-09

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P950005 2001-10-05 CELSIUS DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER Biosense Webster, Inc.

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