FDA UDI In Commercial Distribution 🇺🇸 United States

LineLogic™

DI: 00851780008102 · Model: LL-M-7 · SMD Manufacturing LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
LineLogic™
Primary DI
00851780008102
Version / Model
LL-M-7
Company Name
SMD Manufacturing LLC
Labeler DUNS
070849038
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-01
Public Version
1
Public Version Date
2022-08-09
Public Version Status
New
Public Device Record Key
7d870eff-da61-4816-9467-efe17a0289a4

Device Description

Sterile, Linelogic™ 7 Fr Catheter Stabilization Device

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
KMK Device, Intravascular Catheter Securement

GMDN Terms

Code Name
56631 Wearable percutaneous catheter/tube holder

Identifiers

Type ID
Package 10851780008109
Primary 00851780008102
Package 20851780008106
Package 30851780008103

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 7 French