Primary Device ID | 05707480121748 |
NIH Device Record Key | f12c9aa6-37b6-4624-be42-2833f1d3b0cb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Compression Unit Set, 400 ml, with Clamp |
Version Model Number | 418000400 |
Company DUNS | 305682023 |
Company Name | Ambu A/S |
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 | true |
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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