Primary Device ID | 28800145508661 |
NIH Device Record Key | f96b9bcb-f257-4054-90db-853c37f54db0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rejubeau Fine Meso Needle 34G x 4mm |
Version Model Number | FDND 59 |
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 | 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 | 08800145508667 [Unit of Use] |
GS1 | 18800145508664 [Primary] |
GS1 | 28800145508661 [Package] Contains: 18800145508664 Package: outbox [1000 Units] In Commercial Distribution |
GS1 | 38800145508668 [Package] Package: carton box [5000 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 | 2024-05-17 |
Device Publish Date | 2024-05-09 |