FDA UDI In Commercial Distribution 🇺🇸 United States

Pacific™ Plus

DI: 08033477072203 · Model: PCP050040200 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pacific™ Plus
Primary DI
08033477072203
Version / Model
PCP050040200
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-12
Public Version
1
Public Version Date
2023-10-20
Public Version Status
New
Public Device Record Key
02770547-1c75-475e-b327-931c1c711795

Device Description

CATH PCP050040200 PLUS US D5L40UL2000

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
LIT Catheter, angioplasty, peripheral, transluminal

GMDN Terms

Code Name
17184 Peripheral angioplasty balloon catheter, basic

Identifiers

Type ID
Primary 08033477072203

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K202800 000

Device Sizes

Type Value Unit Text
Length 40.0 Millimeter
Outer Diameter 5.0 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at controlled room temperature, in a dry place. Keep away from sunlight. Do not expose to organic solvents (such as alcohol), ionizing radiation, or ultraviolet light.