Primary Device ID | 06975816240053 |
NIH Device Record Key | f066602f-f17a-42b3-9de4-86ba70d7672b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bawmed |
Version Model Number | BM-SJ-2L-02 |
Company DUNS | 542992754 |
Company Name | SUZHOU BAW MEDTECH 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 | 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 | 06975816240053 [Primary] |
KDQ | Bottle, Collection, Vacuum |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-05 |
Device Publish Date | 2023-05-26 |
06975816240008 | BM-DS wall |
06975816240053 | BM-SJ-2L-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BAWMED 87374832 5353968 Live/Registered |
wenjuan gu 2017-03-17 |