Primary Device ID | 08800024202952 |
NIH Device Record Key | 6ce08c6b-6fae-4ef0-878f-c66e48020a34 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Delikit Medium Body |
Version Model Number | Delikit Medium Body (50ml * 4 Cartridges) |
Company DUNS | 557822311 |
Company Name | Sherpakorea |
Device Count | 1 |
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 |
Phone | +827078429961 |
happidenco@naver.com | |
Phone | +827078429961 |
happidenco@naver.com | |
Phone | +827078429961 |
happidenco@naver.com | |
Phone | +827078429961 |
happidenco@naver.com | |
Phone | +827078429961 |
happidenco@naver.com | |
Phone | +827078429961 |
happidenco@naver.com | |
Phone | +827078429961 |
happidenco@naver.com | |
Phone | +827078429961 |
happidenco@naver.com | |
Phone | +827078429961 |
happidenco@naver.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800024202952 [Primary] |
ELW | Material, Impression |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-08-26 |
Device Publish Date | 2021-08-18 |
08800024201566 | Delikit Medium Body (50ml * 200 Cartridges) |
08800024201542 | Delikit Medium Body (50ml * 2 Cartridges) |
08800024201870 | Delikit Medium Body (50ml * 50 Cartridges) |
08800024202952 | Delikit Medium Body (50ml * 4 Cartridges) |
08800024203201 | Delikit Medium Body (50ml * 10 Cartridges) |