Nimbus Electrosurgical Radiofrequency Multitined Expandable Electrode

8 catalogue numbers from NIM05010BB, listed by Biomerics, United States, under Probe, Radiofrequency Lesion. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
8catalogue numbers in this listing
2510(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 Nimbus Electrosurgical Radiofrequency Multitined Expandable Electrode
Listed by Biomerics, United States
FDA product code GXI
Device type Probe, Radiofrequency Lesion
Device class Class 2
Regulation 21 CFR 882.4725
Establishment Contract manufacturer, Manufacturer
Record published 2018-03-03
Record revised 2023-05-03 (version 5)

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

Catalogue Numbers

Catalogue numbers for Nimbus Electrosurgical Radiofrequency Multitined Expandable Electrode
Catalogue number Size Per pack Status
NIM05010BB 10 In distribution
NIM05010BB In distribution
NIM15010BB In distribution
NIM15010BB 10 In distribution
NIM10010BB 10 In distribution
NIM10010BB In distribution
NIM10010BBCS In distribution
NIM10010BBCS 10 In distribution

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
cannulaCC Cosman Medical, Inc. 47

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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K190259 2020-02-07
K121773 2012-09-21

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