Primary Device ID | 06924607702782 |
NIH Device Record Key | 54588041-c02f-45f0-9ea8-0c5c37a94db1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Transcutaneous Electrical Nerve Stimulator |
Version Model Number | KTR-4037 |
Company DUNS | 544395368 |
Company Name | Shenzhen Kentro Medical Electronics Co.,Ltd |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
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 | 06924607702782 [Primary] |
NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-11 |
Device Publish Date | 2023-12-01 |
06924607701624 | KTR-206 |
06924607701617 | KTR-209 |
06924607701600 | KTR-208 |
06924607702652 | KTR-405 |
06924607702911 | KTR-4031 |
06924607702799 | KTR-4039 |
06924607702782 | KTR-4037 |
06924607702775 | KTR-4036 |
06924607702768 | KTR-4034 |
06924607702751 | KTR-4032 |
06924607702744 | KTR-4029 |
06924607702737 | KTR-4027 |
06924607702720 | KTR-4026 |
06924607702713 | KTR-4021 |
06924607702706 | KTR-4015 |
06924607702683 | KTR-4012 |