FDA UDI In Commercial Distribution 🇺🇸 United States

Launcher™

DI: 00763000909666 · Model: LA7LCBSH · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Launcher™
Primary DI
00763000909666
Version / Model
LA7LCBSH
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-27
Public Version
1
Public Version Date
2024-06-04
Public Version Status
New
Public Device Record Key
c35a58bb-6199-4e7b-bad8-da7ff3ffc912

Device Description

CATHETER LA7LCBSH LA 7F 100CM LCB

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 00763000909666

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K230156 000

Device Sizes

Type Value Unit Text
Catheter Gauge 7.0 French
Length 100.0 Centimeter
Device Size Text, specify Curve description 1: LCB
Device Size Text, specify Curve description 2: SH

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight