FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00643169072664 · Model: 8543 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00643169072664
Version / Model
8543
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
40faf780-fad8-4731-b7d1-4a5c650d2465

Device Description

KIT 8543 ISOMED CAP IP20.1 PUMP US MKT

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
LKK PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

GMDN Terms

Code Name
44063 Neurosurgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 00643169072664

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P990034 025