FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00763000029630 · Model: 23067 · MEDTRONIC PS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00763000029630
Version / Model
23067
Company Name
MEDTRONIC PS MEDICAL, INC.
Labeler DUNS
089055867
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-08
Public Version
1
Public Version Date
2020-03-16
Public Version Status
New
Public Device Record Key
6aa42333-c9f1-48ce-a3b2-fb45d46a5a48

Device Description

ADAPTER 23067 PREIMPLANT TEST SNAP ASSY

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
LKG Port & catheter, implanted, subcutaneous, intraventricular

GMDN Terms

Code Name
61120 Cerebrospinal fluid shunt adaptor

Identifiers

Type ID
Primary 00763000029630

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K874498 000