FDA UDI In Commercial Distribution 🇺🇸 United States

Pro's Combo V™

DI: 00634782095772 · Model: 728-619-11AR · 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
00634782095772
Version / Model
728-619-11AR
Catalog Number
728-619-11AR
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
d7346bf3-7242-4eb9-9af6-6de67c62008d

Device Description

Pro's Combo Plus 720/619, Adult, Red, 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
DXQ Blood Pressure Cuff
LDE Stethoscope, Manual

GMDN Terms

Code Name
16156 Aneroid manual sphygmomanometer
13755 Mechanical stethoscope

Identifiers

Type ID
Package 00634782597153
Primary 00634782095772

Customer Contacts

Device Sizes

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

Storage Conditions

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