Primary Device ID | 38809407786585 |
NIH Device Record Key | ed0c4b41-ab8a-43ca-a04f-4f43728d5eba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ELASTY Mesoneedle 33Gx4mm |
Version Model Number | FDN 64 |
Company DUNS | 688432407 |
Company Name | Feeltech Co.,Ltd. |
Device Count | 100 |
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 | 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 | 08809407786584 [Unit of Use] |
GS1 | 18809407786581 [Primary] |
GS1 | 28809407786588 [Package] Contains: 18809407786581 Package: [1000 Units] In Commercial Distribution |
GS1 | 38809407786585 [Package] Contains: 28809407786588 Package: [5000 Units] In Commercial Distribution |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-13 |
Device Publish Date | 2019-11-05 |