Primary Device ID | 06936841208098 |
NIH Device Record Key | 6ec9d284-8c8f-4c79-b355-59d27bb76a21 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IV cannula |
Version Model Number | II-B-18G |
Catalog Number | 175005 |
Company DUNS | 418642903 |
Company Name | Tianck Medical Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 06936841208098 [Primary] |
GS1 | 16936841208095 [Package] Package: middle package [125 Units] In Commercial Distribution |
GS1 | 26936841208092 [Package] Contains: 16936841208095 Package: outer package [10 Units] In Commercial Distribution |
FGY | Cannula, Injection |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-05-19 |
Device Publish Date | 2023-02-06 |
06971162816881 | Y type |
06971162816874 | Y type |
06971162816867 | Y type |
06971162816850 | Y type |
06971162816843 | Y type |
06971162812234 | 18G |
06971162812227 | 20G |
06971162812210 | 22G |
06971162812203 | 24G |
06971162812197 | 26G |
06936841208098 | II-B-18G |