Primary Device ID | 20853113007022 |
NIH Device Record Key | 69d8648b-bceb-4590-acba-b603f7b8b84e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GoWISE USA |
Version Model Number | GW22051 |
Company DUNS | 005175432 |
Company Name | MING'S MARK INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
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 | 00853113007028 [Primary] |
GS1 | 10853113007025 [Package] Contains: 00853113007028 Package: [1 Units] In Commercial Distribution |
GS1 | 20853113007022 [Package] Contains: 10853113007025 Package: [12 Units] In Commercial Distribution |
OFE | Central Venous Blood Pressure Kit |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-12-06 |