FDA UDI In Commercial Distribution 🇺🇸 United States

Launcher

DI: 00613994834829 · Model: LA7ECR40 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Launcher
Primary DI
00613994834829
Version / Model
LA7ECR40
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-08
Public Version
9
Public Version Date
2023-09-01
Public Version Status
Update
Public Device Record Key
8e8a6453-9bb0-4c42-8905-761b5f59f2aa

Device Description

CATHETER LA7ECR40 LA 7F 100CM ECR40

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQY CATHETER, PERCUTANEOUS

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Primary 00613994834829

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K022764 000

Device Sizes

Type Value Unit Text
Length 100.0 Centimeter
Device Size Text, specify Curve ECR4.0
Catheter Gauge 7.0 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store catheters straight in a cool dark area. Do not expose catheters to solvents or ionizing radiation.