Primary Device ID | 06970935830567 |
NIH Device Record Key | 72ac6736-8a28-49b7-a28a-6c1475ba3c0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KONMED /Pelvifine |
Version Model Number | KM530B |
Company DUNS | 544436531 |
Company Name | Shenzhen Konmed Technology Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06970935830567 [Primary] |
KPI | Stimulator, Electrical, Non-Implantable, For Incontinence |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-01 |
Device Publish Date | 2022-08-24 |
06970935830543 | This Biofeedback Nerve and Muscle Stimulator is a new type of biofeedback and neuromuscular elec |
06970935830536 | This Biofeedback Nerve and Muscle Stimulator is a new type of biofeedback and neuromuscular elec |
06970935830598 | This Biofeedback device is a type of biofeedback and neuromuscular electrical stimulation therap |
06970935830581 | This Biofeedback device is a type of biofeedback and neuromuscular electrical stimulation therap |
06970935830574 | This Biofeedback device is a type of biofeedback and neuromuscular electrical stimulation therap |
06970935830567 | This Biofeedback device is a type of biofeedback and neuromuscular electrical stimulation therap |