FDA UDI In Commercial Distribution 🇺🇸 United States

DirectVision

DI: 00855308006014 · Model: MA100180 · PERCUVISION LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DirectVision
Primary DI
00855308006014
Version / Model
MA100180
Company Name
PERCUVISION LLC
Labeler DUNS
015755434
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
9
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
3bcd90b7-3378-4944-97b7-9dbbf07b03d6

Device Description

18 Fr. Coude tip Foley catheter for DirectVision System

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No
Sterilization Methods
Ultraviolet Light

Product Codes

Code Name
EZL Catheter, Retention Type, Balloon

GMDN Terms

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

Identifiers

Type ID
Package 10855308006011
Primary 00855308006014

Premarket Submissions

Submission Number Supplement Number
K110214 000

Device Sizes

Type Value Unit Text
Catheter Gauge 18 French