| Primary Device ID | 06970935830529 |
| NIH Device Record Key | 4d14f8d0-18e7-48c8-8842-cea266414ec8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KONMED /Pelvifine |
| Version Model Number | KM508B |
| Company DUNS | 544436531 |
| Company Name | Shenzhen Konmed Technology Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 | 06970935830529 [Primary] |
| KXQ | Vibrator For Therapeutic Use, Genital |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2026-02-26 |
| Device Publish Date | 2025-09-30 |
| 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 |
| 06970935830529 | Kegel exercise trainer |