FDA UDI In Commercial Distribution 🇺🇸 United States

GENTLECATH GLIDE

DI: 00768455168781 · Model: 510482 · CONVATEC, PURCHASING DEPARTMENT
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GENTLECATH GLIDE
Primary DI
00768455168781
Version / Model
510482
Company Name
CONVATEC, PURCHASING DEPARTMENT
Labeler DUNS
809784593
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-30
Public Version
1
Public Version Date
2023-11-07
Public Version Status
New
Public Device Record Key
02eca643-95f3-420a-8c34-c7e7e9c972f7

Device Description

GentleCath™ Glide Intermittent Urinary Catheter

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
GBM CATHETER, URETHRAL

GMDN Terms

Code Name
45603 Single-administration urethral drainage catheter

Identifiers

Type ID
Package 00768455168613
Primary 00768455168781
Package 00768455168958

Customer Contacts

Phone
+18004228811

Premarket Submissions

Submission Number Supplement Number
K181206 000