FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00643169495814 · Model: 20MRK · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00643169495814
Version / Model
20MRK
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-05-08
Public Version
5
Public Version Date
2020-05-06
Public Version Status
Update
Public Device Record Key
7292875b-4cc7-4b9c-b6bc-59b2898da9dc

Device Description

KIT 20MRK ARCTIC FRNT MANETRACT GLB ROHS

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

GMDN Terms

Code Name
17541 Catheter/overtube balloon inflator, single-use

Identifiers

Type ID
Primary 00643169495814

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P100010 047

Storage Conditions

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