FDA UDI In Commercial Distribution 🇺🇸 United States

Diagnostix™

DI: 00634782009229 · Model: 805 · AMERICAN DIAGNOSTIC CORP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Diagnostix™
Primary DI
00634782009229
Version / Model
805
Catalog Number
805
Company Name
AMERICAN DIAGNOSTIC CORP
Labeler DUNS
108999095
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
1135b990-1dcb-4c09-9322-efd85042069c

Device Description

Gauge-750, 752,White

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXQ Blood Pressure Cuff

GMDN Terms

Code Name
16156 Aneroid manual sphygmomanometer

Identifiers

Type ID
Primary 00634782009229
Package 00634782509170

Customer Contacts

Storage Conditions

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