FDA UDI Not in Commercial Distribution 🇺🇸 United States

REEF HP

DI: 08033477063324 · Model: REE070080122 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REEF HP
Primary DI
08033477063324
Version / Model
REE070080122
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-23
Public Version
5
Public Version Date
2019-08-09
Public Version Status
Update
Public Device Record Key
5c1e55da-cff9-4e8d-95d6-6970606730af
Distribution End Date
2018-10-05

Device Description

CATH REE070080122 REEUS 07.00 L080UL1200

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
DQY CATHETER, PERCUTANEOUS

GMDN Terms

Code Name
17184 Peripheral angioplasty balloon catheter, basic

Identifiers

Type ID
Primary 08033477063324

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K092361 000

Device Sizes

Type Value Unit Text
Length 80.0 Millimeter
Outer Diameter 7.0 Millimeter

Storage Conditions

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