Primary Device ID | B040CPH250 |
NIH Device Record Key | d4d6870a-e098-44e0-9caa-a7c0193e230c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Coronary Artery Probe 2.50mm |
Version Model Number | CPH-2.50 |
Company DUNS | 939872651 |
Company Name | GENESEE BIOMEDICAL, 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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B040CPH250 [Package] Contains: B040CPH2500 Package: [1 Units] In Commercial Distribution |
HIBCC | B040CPH2500 [Primary] |
DWS | Instruments, Surgical, Cardiovascular |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B040CPH250]
Moist Heat or Steam Sterilization
[B040CPH250]
Moist Heat or Steam Sterilization
[B040CPH250]
Moist Heat or Steam Sterilization
[B040CPH250]
Moist Heat or Steam Sterilization
[B040CPH250]
Moist Heat or Steam Sterilization
[B040CPH250]
Moist Heat or Steam Sterilization
[B040CPH250]
Moist Heat or Steam Sterilization
[B040CPH250]
Moist Heat or Steam Sterilization
[B040CPH250]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-13 |
Device Publish Date | 2024-12-05 |
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B040ARC9 - Aortic Repair Caliper | 2024-12-13 Aortic Repair Tool Kit - Cusp Calipers |
B040ASR19210 - Annular Sizer Aortic | 2024-12-13 Aortic Repair Tool Kit - Annular Sizers |
B040ASR2325 - Annular Sizer Aortic | 2024-12-13 Aortic Repair Tool Kit - Annular Sizers |
B040ASR2729 - Annular Sizer Aortic | 2024-12-13 Aortic Repair Tool Kit - Annular Sizers |