FDA UDI In Commercial Distribution 🇺🇸 United States

InstantCath

DI: 00610075104413 · Model: 9672 · HOLLISTER INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
30

Basic Information

Brand Name
InstantCath
Primary DI
00610075104413
Version / Model
9672
Catalog Number
9672
Company Name
HOLLISTER INCORPORATED
Labeler DUNS
005527098
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2024-07-09
Public Version
1
Public Version Date
2024-07-17
Public Version Status
New
Public Device Record Key
c671ed7a-cea2-4068-8e75-186096ca2f8c

Device Description

Pre-lubricated Urethral Intermittent 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
Yes
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 20610075104417
Primary 00610075104413
Unit of Use 00610075067183

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K011552 000

Device Sizes

Type Value Unit Text
Catheter Length 40 Centimeter
Catheter Gauge 14 French