Primary Device ID | 28809407787011 |
NIH Device Record Key | 7190119b-0530-45d9-ac39-73cfb210ea80 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IDryNeedle 0.25x30 |
Version Model Number | DN150 0.25x30 |
Company DUNS | 688432407 |
Company Name | Feeltech Co.,Ltd. |
Device Count | 100 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08809407787017 [Unit of Use] |
GS1 | 18809407787014 [Primary] |
GS1 | 28809407787011 [Package] Contains: 18809407787014 Package: Carton box [20000 Units] In Commercial Distribution |
GS1 | 38809407787018 [Package] Package: CARTONBOX [20000 Units] In Commercial Distribution |
MQX | Needle, Acupuncture, Single Use |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-23 |
Device Publish Date | 2020-01-15 |