Primary Device ID | 06970442090027 |
NIH Device Record Key | 18068bfc-bd6d-4588-b0fe-803501358073 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VCOMIN Fetal Doppler |
Version Model Number | FD-231B |
Company DUNS | 548312355 |
Company Name | Vcomin Technlogy Limited |
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 | 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 | 06970442090027 [Primary] |
GS1 | 16970442090024 [Package] Package: box [30 Units] In Commercial Distribution |
KNG | Monitor, Ultrasonic, Fetal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-23 |
Device Publish Date | 2020-07-15 |
06970442090256 | FD-610G |
06970442090249 | FD-610B |
06970442090232 | FD-590G |
06970442090225 | FD-590B |
06970442090218 | FD-510G |
06970442090201 | FD-510B |
06970442090171 | FD-200D |
06970442090164 | FD-200B |
06970442090096 | FD-500G |
06970442090089 | FD-500B |
06970442090072 | FD-640D |
06970442090065 | FD-640B |
06970442090058 | FD-591D |
06970442090041 | FD-591B |
06970442090027 | FD-231B |
00697044209003 | FD-231D |
16970442090000 | FD-540B |
16970442090284 | FD-540C |
16970442090277 | FD-540D |
16970442090260 | FD-540G |
16970442090031 | FD-231D |
16970442090383 | FD-570G |
16970442090376 | FD-570B |
16970442090369 | FD-290G |
16970442090352 | FD-290B |
16970442090345 | FD-260G |
16970442090338 | FD-260B |