Primary Device ID | 38809407786806 |
NIH Device Record Key | 2f2b1f34-705b-4bc7-8aaf-fb00af5d6d25 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Miracu FC BI 19Gx90mm |
Version Model Number | F-FTN1991G |
Company DUNS | 688432407 |
Company Name | Feeltech Co.,Ltd. |
Device Count | 10 |
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 | 08809407786805 [Unit of Use] |
GS1 | 18809407786802 [Primary] |
GS1 | 28809407786809 [Package] Contains: 18809407786802 Package: INBOX [10 Units] In Commercial Distribution |
GS1 | 38809407786806 [Package] Contains: 28809407786809 Package: CARTON BOX [300 Units] In Commercial Distribution |
NEW | Suture, Surgical, Absorbable, Polydioxanone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2021-02-05 |
Device Publish Date | 2019-12-24 |