FDA UDI In Commercial Distribution 🇺🇸 United States

GentleCath Hydrophilic

DI: 07333387031729 · Model: 508990 · Wellspect AB
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
GentleCath Hydrophilic
Primary DI
07333387031729
Version / Model
508990
Catalog Number
508990
Company Name
Wellspect AB
Labeler DUNS
351118942
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-01
Public Version
5
Public Version Date
2024-12-12
Public Version Status
Update
Public Device Record Key
bc7beaae-8732-4b05-8901-52f671830c2c

Device Description

Hydrophilic Intermittent Urinary Catheter With Water Sachet Female 8'' 12FR

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
Yes
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 07333387031743
Package 07333387031736
Primary 07333387031729
Previous 00768455142583

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 12 French
Length 8 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry