FDA UDI In Commercial Distribution 🇺🇸 United States

GENTLECATH

DI: 00768455168798 · Model: 510483 · CONVATEC, PURCHASING DEPARTMENT
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GENTLECATH
Primary DI
00768455168798
Version / Model
510483
Company Name
CONVATEC, PURCHASING DEPARTMENT
Labeler DUNS
809784593
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-26
Public Version
3
Public Version Date
2023-10-30
Public Version Status
Update
Public Device Record Key
845f843a-5cc0-48fc-a07c-89b75b598387

Device Description

GENTLECATH GLIDE MALE CH14 (1x10PK) US

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 00768455168965
Package 00768455168620
Primary 00768455168798

Customer Contacts

Phone
+18004228811