FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00763000593889 · Model: NITRONRMT · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
00763000593889
Version / Model
NITRONRMT
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-17
Public Version
1
Public Version Date
2024-02-26
Public Version Status
New
Public Device Record Key
fe23eb81-2ba3-40fb-a60e-2ef16b5c853a

Device Description

REMOTE NITRONRMT GLOBAL

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LPB Cardiac ablation percutaneous catheter

GMDN Terms

Code Name
60721 Cardiac cryosurgical system

Identifiers

Type ID
Primary 00763000593889

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P020045 105

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry