Primary Device ID | 07350109400137 |
NIH Device Record Key | d0e57b87-6c28-4f9d-90b3-a9abad4276e5 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 15966-92 |
Catalog Number | 1596692 |
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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