FDA UDI In Commercial Distribution 🇺🇸 United States

FLUME catheter

DI: 05060894850056 · Model: FLUME catheter 16Fr · THE FLUME CATHETER COMPANY LIMITED
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
FLUME catheter
Primary DI
05060894850056
Version / Model
FLUME catheter 16Fr
Catalog Number
1005
Company Name
THE FLUME CATHETER COMPANY LIMITED
Labeler DUNS
221621138
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-14
Public Version
1
Public Version Date
2024-11-22
Public Version Status
New
Public Device Record Key
d5849cbc-94ae-4ed9-8eb1-0883d4406f3c

Device Description

FLUME catheter 375mm 16Fr

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EZL Catheter, Retention Type, Balloon
KOB Catheter, Suprapubic (And Accessories)

GMDN Terms

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

Identifiers

Type ID
Primary 05060894850056
Package 15060894850053
Package 25060894850050

Customer Contacts