Primary Device ID | 26938634490219 |
NIH Device Record Key | 89ba41ce-ba7a-47d5-bcd3-682eca5c5e0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Able Central Venous Catheter Double Lumen 5F*5cm |
Version Model Number | 02X-FV-2521 |
Company DUNS | 547055364 |
Company Name | Guangdong Baihe Medical Technology Co., Ltd. |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06938634490215 [Primary] |
GS1 | 16938634490212 [Package] Contains: 06938634490215 Package: [10 Units] In Commercial Distribution |
GS1 | 26938634490219 [Package] Contains: 16938634490212 Package: [40 Units] In Commercial Distribution |
FOZ | Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-20 |