Primary Device ID | 16974564883663 |
NIH Device Record Key | bddf57f9-7be6-464e-bb57-11708ecb1a95 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bloomden |
Version Model Number | 95×16 ST-C-A3.5 |
Company DUNS | 712529058 |
Company Name | Bloomden Bioceramics (Hunan) 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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 16974564883663 [Primary] |
EIH | Powder, Porcelain |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-30 |
Device Publish Date | 2024-10-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BLOOMDEN 97588197 not registered Live/Pending |
BLOOMDENÂ BIOCERAMICS CO., LTD 2022-09-12 |
BLOOMDEN 87017809 5100002 Live/Registered |
BLOOMDEN BIOCERAMICS CO., LTD 2016-04-28 |