FDA UDI In Commercial Distribution 🇺🇸 United States

TREK

DI: 08717648138348 · Model: 1012273-08 · ABBOTT VASCULAR INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TREK
Primary DI
08717648138348
Version / Model
1012273-08
Catalog Number
1012273-08
Company Name
ABBOTT VASCULAR INC.
Labeler DUNS
964569052
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-02-19
Public Version
5
Public Version Date
2020-03-23
Public Version Status
Update
Public Device Record Key
dd1597b1-dc49-4948-aac0-f0c47275e7c7

Device Description

TREK Coronary Dilatation Catheter 2.75 mm x 8 mm / Rapid-Exchange

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
Labeling does not contain MRI Safety Information
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
LOX Catheters, transluminal coronary angioplasty, percutaneous

GMDN Terms

Code Name
47732 Coronary angioplasty balloon catheter, basic

Identifiers

Type ID
Primary 08717648138348

Customer Contacts

Storage Conditions

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