Primary Device ID | 10815149025329 |
NIH Device Record Key | 8cc4e9d2-c3cf-4b71-8397-8d585c247a16 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Navigator Bionavigation System |
Version Model Number | 60-3020 |
Catalog Number | 60-3020 |
Company DUNS | 147530323 |
Company Name | CORPAK MEDSYSTEMS, 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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(847)403-3400 |
questions@corpak.com | |
Phone | +1(847)403-3400 |
questions@corpak.com | |
Phone | +1(847)403-3400 |
questions@corpak.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10815149025329 [Primary] |
FOZ | Catheter,intravascular,therapeutic,short-term less than 30 days |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-05-19 |
Device Publish Date | 2016-08-04 |
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20815149022882 - CORFLO cuBBy Right Angle Feeding Set | 2023-07-31 Feeding set for use with CORFLO cuBBy with ENFit connectors |
20815149024442 - CORFLO cuBBy | 2023-07-31 Feeding set for use with CORFLO cuBBy |