FDA UDI Not in Commercial Distribution 🇺🇸 United States

HDMD PRO

DI: 00817613020512 · Model: HDMD PRO · MED X CHANGE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HDMD PRO
Primary DI
00817613020512
Version / Model
HDMD PRO
Company Name
MED X CHANGE, INC.
Labeler DUNS
051244569
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-26
Public Version
4
Public Version Date
2020-05-19
Public Version Status
Update
Public Device Record Key
97d3b1e8-b413-4d09-8eae-858cb8ffda15
Distribution End Date
2018-11-08

Device Description

HDMD PRO

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LMB Device, Digital Image Storage, Radiological

GMDN Terms

Code Name
18034 Endoscopic video image processing unit

Identifiers

Type ID
Primary 00817613020512

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
94 – Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Handling Environment Temperature
Temperature Range
0 – 26 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
85 – Percent (%) Relative Humidity
Type
Handling Environment Atmospheric Pressure
Temperature Range
85 – 105 KiloPascal