FDA UDI In Commercial Distribution 🇺🇸 United States

Pro's Combo V™

DI: 00634782095802 · Model: 728-619-11ATL · AMERICAN DIAGNOSTIC CORP
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pro's Combo V™
Primary DI
00634782095802
Version / Model
728-619-11ATL
Catalog Number
728-619-11ATL
Company Name
AMERICAN DIAGNOSTIC CORP
Labeler DUNS
108999095
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-02
Public Version
1
Public Version Date
2020-01-10
Public Version Status
New
Public Device Record Key
e5aae111-661d-479b-878f-3d3cdd1ce7f0

Device Description

Pro's Combo Plus 720/619, Adult, Teal, Disp pkg

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LDE Stethoscope, Manual
DXQ Blood Pressure Cuff

GMDN Terms

Code Name
13755 Mechanical stethoscope
16156 Aneroid manual sphygmomanometer

Identifiers

Type ID
Package 00634782597184
Primary 00634782095802

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Adult, 23-40cm

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-4 – 131 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
15 – 85 Percent (%) Relative Humidity