FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00763000181215 · Model: 5103 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00763000181215
Version / Model
5103
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-14
Public Version
3
Public Version Date
2022-08-31
Public Version Status
Update
Public Device Record Key
b029c004-7dbd-4ea6-9c2c-319efdd91e8d

Device Description

ADAPTOR CABLE 5103

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
LWP Implantable pulse generator, pacemaker (non-CRT)
DXY implantable pacemaker Pulse-generator

GMDN Terms

Code Name
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Primary 00763000181215

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P890003 437

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
– 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius