FDA UDI In Commercial Distribution 🇺🇸 United States

Magic3™ Intermittent Catheter

DI: 00801741068348 · Model: 52308 · C. R. Bard, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Magic3™ Intermittent Catheter
Primary DI
00801741068348
Version / Model
52308
Catalog Number
52308
Company Name
C. R. Bard, Inc.
Labeler DUNS
016898496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-26
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
1e661f72-9742-446d-b7e2-23ed65e8b909

Device Description

Magic3™ Intermittent Catheter, Pediatric

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
KOD CATHETER, UROLOGICAL

GMDN Terms

Code Name
45603 Single-administration urethral drainage catheter

Identifiers

Type ID
Package 10801741068345
Primary 00801741068348
Package 20801741068342

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 8 French