Primary Device ID | 04022495824943 |
NIH Device Record Key | 8333733e-374f-4bc8-92f8-a0a270f49339 |
Commercial Distribution Discontinuation | 2020-02-26 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | B.BRAUN |
Version Model Number | 7B3116 |
Catalog Number | 7B3116 |
Company DUNS | 002397347 |
Company Name | B. BRAUN MEDICAL INC. |
Device Count | 100 |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
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