FDA UDI In Commercial Distribution 🇺🇸 United States

Autoinjector 2

DI: 00850007370398 · Model: TV-AI01-N · Endologix, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Autoinjector 2
Primary DI
00850007370398
Version / Model
TV-AI01-N
Catalog Number
TV-AI01-N
Company Name
Endologix, Inc.
Labeler DUNS
179593652
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-28
Public Version
1
Public Version Date
2023-03-08
Public Version Status
New
Public Device Record Key
f440b4cd-3b3c-49b4-bf0d-8b7997accf7e

Device Description

"The Autoinjector 2 is a component of the Alto™ Abdominal Stent Graft System. The Autoinjector 2 applies controlled force to the syringe plunger of the CustomSeal Kit to inject the fill polymer into the graft until pressure equilibrium is reached and complete fill of the primary sealing ring, fill channels, and support rings in the graft material the of the aortic body is achieved."

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MIH System, Endovascular Graft, Aortic Aneurysm Treatment

GMDN Terms

Code Name
46777 Abdominal aorta endovascular stent-graft

Identifiers

Type ID
Primary 00850007370398

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P120006 031

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place.