FDA UDI In Commercial Distribution 🇺🇸 United States

Quik-Prep

DI: 00812345022780 · Model: 011440-005 · MORTARA INSTRUMENT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Quik-Prep
Primary DI
00812345022780
Version / Model
011440-005
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
4
Public Version Date
2020-06-29
Public Version Status
Update
Public Device Record Key
be81f3d4-3acd-4297-9ba3-e0756fe6218b

Device Description

Electrode application system

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Primary 00812345022780

Customer Contacts

Phone
888-667-8272

Premarket Submissions

Submission Number Supplement Number
K782079 000
K821757 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 185 Degrees Fahrenheit