FDA UDI In Commercial Distribution 🇺🇸 United States

SimPro™ Now

DI: 07392532188671 · Model: 5101000 · Wellspect AB
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
SimPro™ Now
Primary DI
07392532188671
Version / Model
5101000
Catalog Number
5101000
Company Name
Wellspect AB
Labeler DUNS
351118942
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-10
Public Version
6
Public Version Date
2024-01-17
Public Version Status
Update
Public Device Record Key
e81a6086-9600-4206-9d3d-057a3c0d3048
Distribution End Date
2024-03-31

Device Description

Single Use Urinary Catheter with water sachet. Male Nelaton 16" 10FR

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EZD CATHETER, STRAIGHT

GMDN Terms

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

Identifiers

Type ID
Package 07392532188695
Package 07392532188688
Primary 07392532188671

Customer Contacts

Device Sizes

Type Value Unit Text
Length 16 Inch
Catheter Gauge 10 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a dry place at room temperature.