Primary Device ID | 00821925004658 |
NIH Device Record Key | 9f3ab93c-0035-4f46-a6d3-b0f95d2c2b5f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 7.0FR (2.3mm) X 24 cm URO-GUIDE ™ URETERAL STENT |
Version Model Number | 5497024 |
Company DUNS | 007198742 |
Company Name | Gyrus Acmi, Inc. |
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 | true |
OTC Over-The-Counter | false |
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