Primary Device ID | 00810024670116 |
NIH Device Record Key | 998d25a1-b800-4013-bd37-9ad0ef4d0bc6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CPS Locator 3D, Large Delivery System |
Version Model Number | 600300407 |
Company DUNS | 117126091 |
Company Name | CENTERPOINT SYSTEMS LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | 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 | 00810024670116 [Primary] |
DQY | Catheter, 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 | 2023-03-27 |
Device Publish Date | 2023-03-17 |
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