Primary Device ID | 26938634491971 |
NIH Device Record Key | dc4519da-3a8d-4347-bd1f-2a99234d700f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Able Central Venous Catheter Double Lumen 5F*8cm |
Version Model Number | 02X-FV-2522 |
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 | 06938634491977 [Primary] |
GS1 | 16938634491974 [Package] Contains: 06938634491977 Package: [10 Units] In Commercial Distribution |
GS1 | 26938634491971 [Package] Contains: 16938634491974 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 |