FDA UDI In Commercial Distribution 🇺🇸 United States

SpeediCath

DI: 05708932698320 · Model: 28702 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SpeediCath
Primary DI
05708932698320
Version / Model
28702
Catalog Number
28702
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-01
Public Version
1
Public Version Date
2022-04-11
Public Version Status
New
Public Device Record Key
40783c7b-0326-468a-99cf-e3ce53de2286

Device Description

Catheter Gauge 12 FR/CH.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GBM CATHETER, URETHRAL

GMDN Terms

Code Name
45605 Single-administration urethral catheterization kit, single-use

Identifiers

Type ID
Package 05708932698337
Primary 05708932698320

Premarket Submissions

Submission Number Supplement Number
K143182 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Descriptive Catheter Length Male
Catheter Length 34 Centimeter
Outer Diameter 0.16 Inch
Catheter Gauge 12 French
Outer Diameter 4 Millimeter
Catheter Length 13.2 Inch
Catheter Working Length 30 Centimeter
Catheter Working Length 11.8 Inch