FDA UDI Not in Commercial Distribution 🇺🇸 United States

SpeediCath Flex Coude Pro

DI: 05708932674744 · Model: 20010 · 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
05708932674744
Version / Model
20010
Catalog Number
20010
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
e8084cbf-25ad-4266-80fd-95dcce8e59f5
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 05708932674751
Primary 05708932674744
Package 05708932674768

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 3.3 Millimeter
Catheter Gauge 10 French
Device Size Text, specify Male
Length 44 Centimeter
Length 17.32 Inch

Storage Conditions

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