Primary Device ID | 28800145503413 |
NIH Device Record Key | 44cd841c-0609-4cac-8d4f-c340bb101f51 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Miracu FCL FORTE FIX 18Gx100mm |
Version Model Number | 3FX18101802GA |
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 | 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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800145503419 [Unit of Use] |
GS1 | 18800145503416 [Primary] |
GS1 | 28800145503413 [Package] Contains: 18800145503416 Package: INBOX [10 Units] In Commercial Distribution |
GS1 | 38800145503410 [Package] 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 | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-02 |
Device Publish Date | 2022-05-25 |