FDA UDI In Commercial Distribution 🇺🇸 United States

CURE ULTRAPLUS CATHETER

DI: 00815947021335 · Model: ULTRAPlus8 · CONVATEC, PURCHASING DEPARTMENT
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
CURE ULTRAPLUS CATHETER
Primary DI
00815947021335
Version / Model
ULTRAPlus8
Company Name
CONVATEC, PURCHASING DEPARTMENT
Labeler DUNS
809784593
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-19
Public Version
4
Public Version Date
2023-04-21
Public Version Status
Update
Public Device Record Key
63dfc1af-174f-4f92-9a69-f70afb06ab88

Device Description

Sterile Female Intermittent Catheter, Straight Tip

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
KOD Catheter, Urological

GMDN Terms

Code Name
45603 Single-administration urethral drainage catheter

Identifiers

Type ID
Primary 00815947021335
Package 10815947021332
Package 20815947021339

Customer Contacts

Phone
+18004228811

Device Sizes

Type Value Unit Text
Catheter Gauge 08 French