Primary Device ID | 20629160000350 |
NIH Device Record Key | 639239ab-7883-4bd2-8222-fb954253731b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FEATHER-FLEX |
Version Model Number | 2L |
Catalog Number | OL-649502-00/NSP0204 |
Company DUNS | 248200149 |
Company Name | BOMImed Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com | |
Phone | 204-633-2664 |
regulatory@bomimed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10629160000346 [Primary] |
GS1 | 20629160000350 [Package] Contains: 10629160000346 Package: case [30 Units] In Commercial Distribution |
BTC | Bag, Reservoir |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-22 |
Device Publish Date | 2025-07-14 |
20629160000305 | 3 LITRE DISPOSABLE LATEX FREE BREATHING BAG |
20629160000350 | 2 LITRE DISPOSABLE LATEX FREE BREATHING BAG |