Primary Device ID | 08806369468862 |
NIH Device Record Key | b8df64bd-e9cc-469b-ac99-556f0ee65cf5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BONASTENT® Tracheal/Bronchial |
Version Model Number | BTB-160409 |
Company DUNS | 687784405 |
Company Name | Sewoon Medical 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 | true |
Donation Id Number | true |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 08806369468862 [Primary] |
JCT | Prosthesis, Tracheal, Expandable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-02-19 |
Device Publish Date | 2017-03-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BONASTENT 77603874 3791959 Live/Registered |
SEWOON Medical Co., Ltd. 2008-10-30 |
BONASTENT 77603874 3791959 Live/Registered |
Standard Sci-Tech Inc. 2008-10-30 |
BONASTENT 77536886 not registered Dead/Abandoned |
EndoChoice, Inc. 2008-08-01 |