FDA UDI In Commercial Distribution 🇺🇸 United States

Freezor® MAX

DI: 00763000245474 · Model: 239F3 · MEDTRONIC, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Freezor® MAX
Primary DI
00763000245474
Version / Model
239F3
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-24
Public Version
1
Public Version Date
2021-01-01
Public Version Status
New
Public Device Record Key
b6719dca-4a6e-4872-a8aa-f47af1877204

Device Description

CATHETER 239F3 FREEZOR MAX3 MED BLUE 9F

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
OAE Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation
LPB Cardiac ablation percutaneous catheter

GMDN Terms

Code Name
60720 Cardiac cryosurgical system catheter

Identifiers

Type ID
Primary 00763000245474

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P100010 098

Device Sizes

Type Value Unit Text
Length 90.0 Centimeter
Device Size Text, specify Catheter shaft size 9 Fr
Device Size Text, specify Catheter curve length 55mm
Device Size Text, specify Catheter tip length 8mm

Storage Conditions

Type
Handling Environment Humidity
Temperature Range
– 85 Percent (%) Relative Humidity
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Storage Environment Temperature
Temperature Range
59 – 86 Degrees Fahrenheit
Type
Handling Environment Temperature
Temperature Range
-31 – 136 Degrees Fahrenheit