Primary Device ID | 04716770254104 |
NIH Device Record Key | 4fdbe8ce-9cab-4be4-ae43-cf3ef5d6c754 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SINGLE USE ADULT 1600ML RESUSCITATOR W/O POP-OFF |
Version Model Number | RE-25410 |
Company DUNS | 658023775 |
Company Name | BESMED HEALTH BUSINESS CORP. |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04716770254104 [Primary] |
BTM | Ventilator, Emergency, Manual (Resuscitator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-05-23 |
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