Primary Device ID | 00724995150587 |
NIH Device Record Key | e6de52b9-d2c1-4a04-9de2-588a0a72bdfb |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | AX06757 |
Catalog Number | AX06757 |
Company DUNS | 813116209 |
Company Name | Steris Mexico, S. de R.L. de C.V. |
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 | false |
OTC Over-The-Counter | true |
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