FDA UDI Not in Commercial Distribution 🇺🇸 United States

Duet®

DI: 00763000428747 · Model: 46913 · MEDTRONIC PS MEDICAL, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Duet®
Primary DI
00763000428747
Version / Model
46913
Company Name
MEDTRONIC PS MEDICAL, INC.
Labeler DUNS
089055867
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-07
Public Version
2
Public Version Date
2023-08-30
Public Version Status
Update
Public Device Record Key
3c011d08-77f3-4e67-aa7d-00c8bc0a00eb
Distribution End Date
2021-12-17

Device Description

EDMS 46913 DUET INTERLINK SITES

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
MR Conditional
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
PCB External cerebrospinal fluid (CSF) diversion
GWM Device, monitoring, intracranial pressure
JXG Shunt, central nervous system and components

GMDN Terms

Code Name
61796 Cerebrospinal fluid external drainage kit

Identifiers

Type ID
Primary 00763000428747

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
DEN120017 000