FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00681490501880 · Model: 9790XLA · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
00681490501880
Version / Model
9790XLA
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-23
Public Version
4
Public Version Date
2019-02-18
Public Version Status
Update
Public Device Record Key
8ad4368e-a2f0-488d-b3c6-fa6e0b4a2163
Distribution End Date
2019-01-25

Device Description

SFTWR 9790XLA LEAD PATIENT LONG 9790 TAC

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
KRG Programmer, pacemaker
OSR Pacemaker/icd/crt non-implanted components

GMDN Terms

Code Name
61438 Cardiac pulse generator reader, home-use

Identifiers

Type ID
Primary 00681490501880

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P890003 027