Primary Device ID | 05055788708674 |
NIH Device Record Key | cb5108a4-5d63-4cc7-9b0e-0fed6c41aa6d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Adult Dual Heated Wire Breathing Circuit 1.6M (63") (Kit 1) |
Version Model Number | 038-31-201U |
Company DUNS | 504406273 |
Company Name | FLEXICARE MEDICAL LIMITED |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05055788708674 [Primary] |
BZE | Heater, Breathing System W/Wo Controller (Not Humidifier Or Nebulizer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-27 |
Device Publish Date | 2016-10-04 |
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