FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00643169498211 · Model: 26020 · MEDTRONIC PS MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00643169498211
Version / Model
26020
Company Name
MEDTRONIC PS MEDICAL, INC.
Labeler DUNS
089055867
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-10
Public Version
4
Public Version Date
2021-07-22
Public Version Status
Update
Public Device Record Key
3342d0f1-867c-4df4-94a9-740a456b44b9

Device Description

CATH 26020 EDM VENT 2.6X4.9 TRANSLUC

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
61399 Intracerebral infusion/drainage catheter, short-term

Identifiers

Type ID
Primary 00643169498211

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K981046 000