Primary Device ID | 00724995203252 |
NIH Device Record Key | 2f94b9be-847e-4b74-b125-3cb87b2ce9be |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | Quick Connect |
Catalog Number | QFC1773E |
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 | 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 | false |
OTC Over-The-Counter | true |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00724995203252 [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 | 2020-12-07 |
Device Publish Date | 2020-11-27 |
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