FDA UDI In Commercial Distribution 🇺🇸 United States

MITRACLIP

DI: 08717648149580 · Model: LFT01ST · ABBOTT VASCULAR INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MITRACLIP
Primary DI
08717648149580
Version / Model
LFT01ST
Catalog Number
LFT01ST
Company Name
ABBOTT VASCULAR INC.
Labeler DUNS
964569052
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-12
Public Version
3
Public Version Date
2019-09-10
Public Version Status
Update
Public Device Record Key
42a091f6-5ca5-42c7-ab08-f4fc9a9b9bd5

Device Description

Lift

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KMK DEVICE, INTRAVASCULAR CATHETER SECUREMENT

GMDN Terms

Code Name
60466 Cardiovascular implant implantation tool base

Identifiers

Type ID
Primary 08717648149580

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Handle with care. After cleaning, cover device to avoid contamination. Keep dry. Keep away from sunlight.