Primary Device ID | 20681490032746 |
NIH Device Record Key | c0350bdd-acec-4e41-b1e7-000e8c275f4d |
Commercial Distribution Discontinuation | 2018-10-24 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Reuter Venturi™ |
Version Model Number | 1070011 |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00681490032742 [Primary] |
GS1 | 20681490032746 [Package] Contains: 00681490032742 Package: PK [5 Units] Discontinued: 2018-10-24 Not in Commercial Distribution |
ETD | TUBE, TYMPANOSTOMY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-02-18 |
Device Publish Date | 2015-07-13 |
20681490032791 | VENT TUBE 1070032 10PK BOBBIN PAIR 1.27 |
20681490032777 | VENT TUBE 1070031 5PK VENTURI BOBB 1.27 |
20681490032746 | VENT TUBE 1070011 5PK VENTURI BOBB 1.02 |
20763000039787 | VENT TUBE 1070032 10PK BOBBIN PAIR 1.27 |
20763000039770 | VENT TUBE 1070031 5PK VENTURI BOBB 1.27 |