FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00763000059347 · Model: 6056M · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00763000059347
Version / Model
6056M
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-22
Public Version
1
Public Version Date
2019-01-22
Public Version Status
New
Public Device Record Key
44d0cf7a-4a5c-4337-afb2-b2e1276d7395

Device Description

LEAD ACC KIT 6056M GLOBAL EIFU

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
DWS INSTRUMENTS, SURGICAL, CARDIOVASCULAR

GMDN Terms

Code Name
46455 Torque manipulation device

Identifiers

Type ID
Primary 00763000059347

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 40 Degrees Celsius