FDA UDI In Commercial Distribution 🇺🇸 United States

H3+

DI: 00817655020433 · Model: H3PLUS-CAD-XXXXX · MORTARA INSTRUMENT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
H3+
Primary DI
00817655020433
Version / Model
H3PLUS-CAD-XXXXX
Company Name
MORTARA INSTRUMENT, INC.
Labeler DUNS
062046149
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-21
Public Version
4
Public Version Date
2020-06-29
Public Version Status
Update
Public Device Record Key
2b3f76f1-1c4c-4fdf-946b-1f59de3c6651

Device Description

Holter Recorder

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
MWJ Electrocardiograph,Ambulatory(Without Analysis)

GMDN Terms

Code Name
35162 Electrocardiographic ambulatory recorder

Identifiers

Type ID
Primary 00817655020433

Customer Contacts

Phone
888-667-8272

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 65 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
– 95 Percent (%) Relative Humidity