FDA UDI In Commercial Distribution 🇺🇸 United States

ClearTract

DI: 00850041415130 · Model: 211410SPT · SILQ Technologies Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ClearTract
Primary DI
00850041415130
Version / Model
211410SPT
Company Name
SILQ Technologies Corporation
Labeler DUNS
089032035
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-21
Public Version
2
Public Version Date
2024-07-12
Public Version Status
Update
Public Device Record Key
7aff11fd-d3da-4dd3-9aa6-c6c56047f55f

Device Description

2-Way 100% Silicone, 14Fr X 10ml, ClearTract SPT Catheter

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
Yes
MRI Safety
MR Safe
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
EZL Catheter, Retention Type, Balloon

GMDN Terms

Code Name
34917 Indwelling urethral drainage balloon catheter, non-antimicrobial

Identifiers

Type ID
Primary 00850041415130