FDA UDI In Commercial Distribution 🇺🇸 United States

Prosphyg™

DI: 00634782094553 · Model: 768-609-11ABK · AMERICAN DIAGNOSTIC CORP
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Prosphyg™
Primary DI
00634782094553
Version / Model
768-609-11ABK
Catalog Number
768-609-11ABK
Company Name
AMERICAN DIAGNOSTIC CORP
Labeler DUNS
108999095
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-31
Public Version
1
Public Version Date
2018-10-01
Public Version Status
New
Public Device Record Key
5fb3312e-aaf6-48b3-a523-f9909c5ae19a

Device Description

Pro's Combo 768/609 Kit,Adult, Black, LF

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
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 00634782595937
Primary 00634782094553

Customer Contacts

Device Sizes

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

Storage Conditions

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