Primary Device ID | 28800145501495 |
NIH Device Record Key | 1fd4e6b6-05aa-4f69-a5de-bacd8b0a30ac |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | V SOFT LINE BARB BLUNT CANNULA L 4D 21Gx60mm |
Version Model Number | L4-FTN2162G |
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 | 08800145501491 [Unit of Use] |
GS1 | 18800145501498 [Primary] |
GS1 | 28800145501495 [Package] Contains: 18800145501498 Package: INBOX [10 Units] In Commercial Distribution |
GS1 | 38800145501492 [Package] Package: CARTONBOX [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 | 2021-08-30 |
Device Publish Date | 2021-08-22 |