FDA UDI In Commercial Distribution 🇺🇸 United States

SpeediCath Flex Coude Pro

DI: 05708932125451 · Model: 20022 · 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
05708932125451
Version / Model
20022
Catalog Number
20022
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-12
Public Version
1
Public Version Date
2019-07-22
Public Version Status
New
Public Device Record Key
bf51c88b-5849-4c79-be26-a9a3ef5c95f9

Device Description

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

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 05708932125468
Primary 05708932125451
Package 05708932125475

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K190620 000

Device Sizes

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

Storage Conditions

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