FDA UDI In Commercial Distribution 🇺🇸 United States

Holter Prep Kit

DI: 10812345029939 · Model: 043272 · MORTARA INSTRUMENT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Holter Prep Kit
Primary DI
10812345029939
Version / Model
043272
Company Name
MORTARA INSTRUMENT, INC.
Labeler DUNS
062046149
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2020-06-29
Public Version Status
Update
Public Device Record Key
28a983cd-0fc7-4e14-9db2-ee264ad76fa3

Device Description

Holter prep kit with AA battery cleared with Vision 5LR recorder

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQK Computer, Diagnostic, Programmable

GMDN Terms

Code Name
35162 Electrocardiographic ambulatory recorder

Identifiers

Type ID
Primary 10812345029939
Package 20812345029936
Package 30812345029933

Customer Contacts

Phone
888-667-8272

Premarket Submissions

Submission Number Supplement Number
K945985 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from heat
Type
Storage Environment Temperature
Temperature Range
– 80 Degrees Fahrenheit