MultiStim Sensor StimuGrip

MultiStim SENSOR StimuGrip Monopolar Stimulation-handle for MultiStim SENSOR w/ball electrode Ø10mm,

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code BXN
Manufacturer City Province Registered as Device types
Suzhou Meccan Import and Export Corp. Suzhou Jiangsu Contract manufacturer 71
Easymed Instruments Co., Ltd. Daliang, Shunde, Foshan Guangdong Contract manufacturer 8

Record

Regulatory record for MultiStim Sensor StimuGrip
Listed by Pajunk Gmbh Medizintechnologie, Germany
FDA product code BXN
Device type Stimulator, Nerve, Battery-Powered
Device class Class 2
Regulation 21 CFR 868.2775
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Private-label distributor, Complaint-file establishment, Manufacturer
Record published 2018-11-19
Record revised 2025-03-17 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number
Distribution end date 2025-03-15

Catalogue Numbers

Catalogue numbers for MultiStim Sensor StimuGrip
Catalogue number Size Status
1151-94-18 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SunMed SunMed Group Holdings, LLC 22
Xavant Technology Xavant Technology (PTY) Ltd 14
Stimuplex® B. Braun Medical Inc. 12
AincA® Anesthesia Associates, Inc. 9
Halyard Avanos Medical, Inc. 8
Avanos Avanos Medical, Inc. 8
Stimpod Xavant Technology (PTY) Ltd 6
Multistim Vario Pajunk Gmbh Medizintechnologie 6
Multistim Sensor Pajunk Gmbh Medizintechnologie 5
MultiStim ECO Pajunk Gmbh Medizintechnologie 4
MultiStim Sensor PatientCable Pajunk Gmbh Medizintechnologie 4
Temena Temena GmbH 2

Showing 12 of 19. All products under Stimulator, Nerve, Battery-Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K162086 2017-01-06
K061172 2006-10-17

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