FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00673978240763 · Model: 25030 · MEDTRONIC PS MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00673978240763
Version / Model
25030
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
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
4fbf75bd-6f3e-49d8-88e2-4d2874d4299e

Device Description

KIT 25030 EDM 46115 46124 46126

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
GWM DEVICE, MONITORING, INTRACRANIAL PRESSURE
JXG Shunt, central nervous system and components

GMDN Terms

Code Name
61798 Ventricular cerebrospinal fluid drainage catheterization kit

Identifiers

Type ID
Primary 00673978240763

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K984053 000