Primary Device ID | 05030267166206 |
NIH Device Record Key | 366b37e7-b606-4fbd-8c9b-b6dfdbeac475 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VENTURI VALVE 40% OXYGEN, RED |
Version Model Number | 1400040 |
Company DUNS | 785952607 |
Company Name | Intersurgical Incorporated |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05030267166190 [Primary] |
GS1 | 05030267166206 [Package] Contains: 05030267166190 Package: [50 Units] In Commercial Distribution |
GS1 | 05030267166213 [Package] Contains: 05030267166190 Package: [200 Units] In Commercial Distribution |
BYF | Mask, Oxygen, Low Concentration, Venturi |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-12 |
Device Publish Date | 2024-04-04 |