AutoSonix 012040

GUDID 20884521058344

Soft-tissue ultrasonic surgical system

Primary Device ID	20884521058344
NIH Device Record Key	5e2c9046-ca4a-4aed-a3e5-565f6e2e5829
Commercial Distribution Discontinuation	2019-10-02
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	AutoSonix
Version Model Number	012040
Catalog Number	012040
Company DUNS	058614483
Company Name	Covidien LP
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	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	true

Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;
Special Storage Condition, Specify	Between 0 and 0 *;

Device Issuing Agency	Device ID
GS1	10884521058347 [Primary]
GS1	20884521058344 [Package] Contains: 10884521058347 Package: CASE [3 Units] Discontinued: 2019-10-02 Not in Commercial Distribution

LFL	Instrument, ultrasonic surgical

Steralize Prior To Use	false
Device Is Sterile	true

Mark Image Registration \| Serial	Company Trademark Application Date
AUTOSONIX 86117298 4514798 Live/Registered	Covidien LP 2013-11-13
AUTOSONIX 75378993 2279945 Live/Registered	COVIDIEN LP 1997-10-24