FDA UDI In Commercial Distribution 🇺🇸 United States

SpeediCath Standard

DI: 05701780209090 · Model: 28484 · Coloplast A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
SpeediCath Standard
Primary DI
05701780209090
Version / Model
28484
Catalog Number
28484
Company Name
Coloplast A/S
Labeler DUNS
305524696
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-25
Public Version
2
Public Version Date
2024-04-18
Public Version Status
Update
Public Device Record Key
ac3d26b6-aa4c-41eb-bd5f-007aaaf0a2fa

Device Description

Catheter with accessories containing: 1 ready to use coated catheter, 1 pair of gloves, 1 drape, 2 aseptic cleansing wipes, 1 SpeediBag® 700 ml urine bag.

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
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
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 05701780209250
Primary 05701780209090

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 14 French
Catheter Working Length 13.9 Inch
Catheter Working Length 35 Centimeter
Device Size Text, specify Tip Type Straight/Nelaton

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight. Do not use if package is damaged and consult IFU.