Primary Device ID | 00724995094133 |
NIH Device Record Key | fbaf110e-f3c2-4bc2-85e9-c31748515b2d |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | C1141E |
Catalog Number | C1141E |
Company DUNS | 202659140 |
Company Name | Corporation Steris Canada |
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 | false |
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 |
Phone | +1(800)548-4873 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00724995094133 [Primary] |
MED | Sterilant, medical devices |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-05 |
Device Publish Date | 2020-09-25 |
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