Primary Device ID | 06945764413519 |
NIH Device Record Key | 684701c2-ba39-4818-a569-b6a3e25046b4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Antmed |
Version Model Number | HBF150 |
Company DUNS | 527221254 |
Company Name | ShenZhen Antmed Co., Ltd |
Device Count | 50 |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com | |
Phone | 9999999999 |
info@antmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06945764402766 [Unit of Use] |
GS1 | 06945764412512 [Primary] |
GS1 | 06945764413519 [Package] Contains: 06945764412512 Package: [4 Units] In Commercial Distribution |
DQO | Catheter, Intravascular, Diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-10-31 |
Device Publish Date | 2017-01-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ANTMED 86771799 5062252 Live/Registered |
SHENZHEN ANTMED CO., LTD 2015-09-29 |