Primary Device ID | 30051131275936 |
NIH Device Record Key | 1daae470-c290-4907-82ab-5cff146ecd2a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 3M™ Vflex™ |
Version Model Number | 1804S |
Catalog Number | 1804S |
Company DUNS | 830016148 |
Company Name | 3M COMPANY |
Device Count | 50 |
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 | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00051131275935 [Unit of Use] |
GS1 | 30051131275936 [Primary] |
MSH | Respirator,surgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-05-06 |
Device Publish Date | 2018-02-21 |
30051131275936 | 3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask 1804S, N95 Small |
30051131275929 | 3M™ VFlex™ Health Care Particulate Respirator and Surgical Mask 1804, N95 |