FDA UDI Not in Commercial Distribution 🇺🇸 United States

Freezor® MAX

DI: 00643169504929 · Model: 229F3 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Freezor® MAX
Primary DI
00643169504929
Version / Model
229F3
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-18
Public Version
4
Public Version Date
2019-06-12
Public Version Status
Update
Public Device Record Key
92b527f5-bbb0-4295-a66c-47cfb64d39c8
Distribution End Date
2019-03-15

Device Description

CATH 229F3 FREEZOR MAX3 SURGICAL MED 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
LPB Cardiac ablation percutaneous catheter

GMDN Terms

Code Name
60720 Cardiac cryosurgical system catheter

Identifiers

Type ID
Primary 00643169504929

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P020045 061

Device Sizes

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

Storage Conditions

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
Type
Handling Environment Humidity
Temperature Range
– 85 Percent (%) Relative Humidity