FDA UDI In Commercial Distribution 🇺🇸 United States

All Silicone Foley Catheter

DI: 06936881196591 · Model: F01B032212 · Well Lead Medical Co.,Ltd
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
All Silicone Foley Catheter
Primary DI
06936881196591
Version / Model
F01B032212
Company Name
Well Lead Medical Co.,Ltd
Labeler DUNS
544811862
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-24
Public Version
1
Public Version Date
2024-06-03
Public Version Status
New
Public Device Record Key
3433a2b1-3d94-4a7a-9919-395d2df61a4c

Device Description

2-way Female 22Fr30-50ml

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
Yes
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
Package 16936881196598
Primary 06936881196591
Package 26936881196595

Premarket Submissions

Submission Number Supplement Number
K082815 000