FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00643169498402 · Model: 24148 · MEDTRONIC PS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
NA
Primary DI
00643169498402
Version / Model
24148
Company Name
MEDTRONIC PS MEDICAL, INC.
Labeler DUNS
089055867
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-14
Public Version
4
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
4fa55a54-9598-4c38-9c3f-d711d28a3e4f

Device Description

CATH 24148 C/P STD 110CM NO MARKERS

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JXG Shunt, central nervous system and components

GMDN Terms

Code Name
61159 Peritoneal/atrial cerebrospinal fluid catheter

Identifiers

Type ID
Primary 00643169498402

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K792005 000

Device Sizes

Type Value Unit Text
Outer Diameter 2.5 Millimeter
Length 110.0 Centimeter