Primary Device ID | 04054685271602 |
NIH Device Record Key | ae1204db-ff69-4131-bb09-2d0bc3cd8357 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Low-pressurehose assembly, 2m, 02 green DISS/ PURITAN BENNET |
Version Model Number | 36334 |
Company DUNS | 342832477 |
Company Name | WEINMANN Emergency Medical Technology GmbH + Co. KG |
Device Count | 1 |
DM Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04054685271602 [Primary] |
BTL | Ventilator, Emergency, Powered (Resuscitator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-12-15 |
Device Publish Date | 2020-12-07 |
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