FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20763000122151 · Model: APU448 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
NA
Primary DI
20763000122151
Version / Model
APU448
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2019-05-10
Public Version
1
Public Version Date
2019-05-20
Public Version Status
New
Public Device Record Key
7b2bfff9-a66d-415c-9a29-a02ecd5e428f

Device Description

AORTIC PUNCH SH 448 SUA

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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
47914 Aorta punch, single-use

Identifiers

Type ID
Primary 20763000122151
Unit of Use 00763000122157

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 4.8 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry
Type
Special Storage Condition, Specify
Special Conditions
Keep away from heat