FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00643169345560 · Model: 990066 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00643169345560
Version / Model
990066
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-07
Public Version
4
Public Version Date
2021-03-16
Public Version Status
Update
Public Device Record Key
b0441bc8-f4f9-4a22-8838-e5588988a487
Distribution End Date
2019-11-08

Device Description

CABLE 990066 ACHIEVE ELECTRICAL GLOBAL

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
DRF CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING

GMDN Terms

Code Name
46355 Cardiac mapping catheter, percutaneous, single-use

Identifiers

Type ID
Primary 00643169345560

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K102588 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius