Primary Device ID | 00616258010489 |
NIH Device Record Key | 020d8aa0-6e5f-4f0f-ad99-a3ffaa096b83 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ASSY,CBL,STRT SW,AUX,25FT,PROV,UDI,BATCH |
Version Model Number | KMA 550IR 25 |
Catalog Number | KMA 550IR 25 |
Company DUNS | 058716649 |
Company Name | BAYER MEDICAL CARE 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 | false |
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 |
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