Primary Device ID | 07323190045150 |
NIH Device Record Key | e72c4a3e-524c-4754-bd59-98df34aa4ec4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Barrier |
Version Model Number | 42331-02 |
Catalog Number | 42331 |
Company DUNS | 631770658 |
Company Name | Mölnlycke Health Care AB |
Device Count | 60 |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07323190045150 [Package] Contains: 07323190045167 Package: [10 Units] In Commercial Distribution |
GS1 | 07323190045167 [Primary] |
GS1 | 07332430952516 [Unit of Use] |
FXX | Mask, 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 | 2016-09-24 |
07332430617644 | 4272-00 |
07332430617606 | 4273-00 |
07332430085078 | 4270-00 |
07332430084804 | 4235-00 |
07323190046058 | 42291-01 |
07323190045990 | 42281-01 |
07323190045938 | 4225-01 |
07323190045907 | 42241-01 |
07323190045181 | 42371-02 |
07323190045150 | 42331-02 |
07323190043330 | 42671-01 |
07323190043279 | 42321-01 |
07323190001118 | 42391-02 |
07323190000913 | 42381-01 |
07323190000760 | 42341-01 |
07323190000647 | 42311-01 |
07323190000586 | 42301-01 |
07323190000524 | 42361-01 |