Primary Device ID | 06958481438734 |
NIH Device Record Key | 3ec34a8e-d707-4721-8541-1eb66f391a0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | POT PTCA Balloon Dilatation Catheter |
Version Model Number | rev01 |
Catalog Number | 833-2506 |
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 | 06958481438734 [Primary] |
LOX | Catheters, Transluminal Coronary Angioplasty, Percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-05-16 |
Device Publish Date | 2023-05-08 |
06958481438802 | rev01 |
06958481438796 | rev01 |
06958481438789 | rev01 |
06958481438772 | rev01 |
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