No

GUDID 16973810850329

Shenzhen Jian Feng Electronic Technology Co., Ltd.

Physical therapy transcutaneous neuromuscular electrical stimulation system
Primary Device ID16973810850329
NIH Device Record Key89b31778-1836-4d91-82f5-242f96a2b3f8
Commercial Distribution StatusIn Commercial Distribution
Brand NameNo
Version Model NumberTA2224C
Company DUNS560082555
Company NameShenzhen Jian Feng Electronic Technology Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com
Phone+1(678)829-7256
Emailsupport@iauvon.com

Device Identifiers

Device Issuing AgencyDevice ID
GS106973810850322 [Primary]
GS116973810850329 [Package]
Contains: 06973810850322
Package: [48 Units]
In Commercial Distribution
GS126973810850326 [Package]
Contains: 06973810850322
Package: [60 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NGXStimulator, Muscle, Powered, For Muscle Conditioning

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-24
Device Publish Date2024-07-16

On-Brand Devices [No]

06973810850049FM-B2404
06973810850063FM-B2406
06973810850056FM-B2405
16973810854242TU3424
16973810853245TUP324
06973810850070FM-B2407
06973810850025FM-B2402
16973810851517FM-B1501A
16973810850091FM-B2409
16973810850084FM-B2403A
16973810850244TU2224
16973810850237TA3224
16973810850220AS9020
16973810850213AS9020
16973810850206AS9020
16973810850190AS9020
16973810850183AS8019
16973810850176AS8016
16973810850169AS8016
16973810850145AS8012C
16973810850138AS8012
16973810850121AS8012
16973810850114AS8012
16973810850107AS8012
16973810850152YK15AB
16973810850251TP2208
16973810850275TU1130
16973810850268AS1080
16973810850299TA2224
16973810850282TA2224
16973810850305TU1130
16973810850329TA2224C
16973810850312FM-B2409
16973810850343TA3224
16973810850367AS8016
16973810850350AS8016
16973810850374AS8019

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