Primary Device ID | ENOU4180US0 |
NIH Device Record Key | 21333050-e060-44a5-a86b-7302e408b83c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dispenser DP 30 |
Version Model Number | 4180US |
Company DUNS | 480610476 |
Company Name | Nouvag AG |
Device Count | 1 |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
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 |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com | |
Phone | +41718466600 |
info@nouvag.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | ENOU4180US0 [Primary] |
FRN | Pump, Infusion |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2023-09-27 |
Device Publish Date | 2017-01-13 |
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H7871140900111000 | Infiltration pump, SET |
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ENOU4180US0 | Infiltration pump |