cannulaCC

Cannula 10cm, 10mm Tip, 21G

Registry build 21.09.26
1manufacturer
47catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code GXI
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24

Record

Regulatory record for cannulaCC
Listed by Cosman Medical, Inc., United States
FDA product code GXI
Device type Probe, Radiofrequency Lesion
Device class Class 2
Regulation 21 CFR 882.4725
Record published 2016-10-19
Record revised 2023-05-03 (version 6)

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, expiry date
Packaging Pack of 10
Distribution end date 2020-08-13

Catalogue Numbers

Catalogue numbers for cannulaCC
Catalogue number Size Status
CC101021 Withdrawn
CC101018 Withdrawn
CC15220Z Withdrawn
CC5222 Withdrawn
CC10521Z Withdrawn
CC101022 Withdrawn
CC15220 Withdrawn
CC5422 Withdrawn
CC10222 Withdrawn
CC151520 Withdrawn
CC151018 Withdrawn
CC202020 Withdrawn
CC151520Z Withdrawn
CC201020 Withdrawn
CC5421 Withdrawn
CC101022Z Withdrawn
CC10518Z Withdrawn
CC151020 Withdrawn
CC20520Z Withdrawn
CC10522 Withdrawn
CC10520Z Withdrawn
CC151020Z Withdrawn
CC51021 Withdrawn
CC101020Z Withdrawn
CC202020Z Withdrawn
CC10521 Withdrawn
CC152020Z Withdrawn
CC15520L Withdrawn
CC15520Z Withdrawn
CC15518 Withdrawn
CC10222Z Withdrawn
CC101021Z Withdrawn
CC101018Z Withdrawn
CC5422Z Withdrawn
CC101020 Withdrawn
CC51021Z Withdrawn
CC15518Z Withdrawn
CC10522Z Withdrawn
CC15520 Withdrawn
CC20520 Withdrawn
CC5421Z Withdrawn
CC10522L Withdrawn
CC151018Z Withdrawn
CC152020 Withdrawn
CC10518 Withdrawn
CC10520 Withdrawn
CC201020Z Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OWL Diros Technology, Inc. 345
Probe, Radiofrequency Lesion Boston Scientific Neuromodulation Corporation 175
Halyard Avanos Medical, Inc. 156
Lccs Lccs Products Limited 101
Epimed Epimed International, Inc. 100
Avanos Avanos Medical, Inc. 89
NeuroTherm™ Neurotherm, Inc. 87
Probe, Radiofrequency Lesion St. Jude Medical 66
cannulaRFK Cosman Medical, Inc. 56
Rftl Pajunk Gmbh Medizintechnologie 54
Radiofrequency (RF) Needle Spectra Medical Devices, LLC 49
Epimed Minta Medical Limited 35

Showing 12 of 85. All products under Probe, Radiofrequency Lesion

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K082012 2008-10-14
K060799 2006-05-02
K053415 2006-04-25
K050084 2005-03-17

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