Primary Device ID | 06958481477405 |
NIH Device Record Key | 51a1cec9-7b39-4e4e-b32e-557ba2b05ee2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tiche PTA Balloon Dilatation Catheter |
Version Model Number | rev01 |
Catalog Number | 34-062013 |
Company DUNS | 421318800 |
Company Name | BrosMed 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 | false |
Expiration Date | true |
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 | 06958481477405 [Primary] |
LIT | Catheter, Angioplasty, Peripheral, Transluminal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-15 |
Device Publish Date | 2023-05-06 |
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