FDA UDI Not in Commercial Distribution 🇺🇸 United States

SpeediCath Flex Coude Pro

DI: 05708932674775 · Model: 20012 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SpeediCath Flex Coude Pro
Primary DI
05708932674775
Version / Model
20012
Catalog Number
20012
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-24
Public Version
2
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
b7268ec2-6858-4cae-a57e-c86bc16e2034
Distribution End Date
2020-06-18

Device Description

Ready to use curved tip male catheter. Sterile urinary catheter for intermittent catheterization.

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

Product Codes

Code Name
GBM CATHETER, URETHRAL

GMDN Terms

Code Name
45603 Single-administration urethral drainage catheter

Identifiers

Type ID
Package 05708932674799
Package 05708932674782
Primary 05708932674775

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Male
Length 44 Centimeter
Catheter Gauge 12 French
Length 17.32 Inch
Outer Diameter 4 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight