FDA UDI In Commercial Distribution 🇺🇸 United States

Diagnostix™

DI: 00634782076719 · Model: 5413-EU · AMERICAN DIAGNOSTIC CORP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Diagnostix™
Primary DI
00634782076719
Version / Model
5413-EU
Catalog Number
5413-EU
Company Name
AMERICAN DIAGNOSTIC CORP
Labeler DUNS
108999095
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-10-28
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
269e4369-cc0c-4c58-b742-924e445d59ea

Device Description

Diagnostix Portable Dermascope,3.5v, LED, Euro

Device Characteristics

Single Use
Yes
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
Yes
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
FSP Loupe, Diagnostic/Surgical

GMDN Terms

Code Name
45084 Ophthalmic/otologic diagnostic set

Identifiers

Type ID
Package 00634782578084
Primary 00634782076719
Unit of Use 00634782024529

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
14 – 131 Degrees Fahrenheit