FDA UDI In Commercial Distribution 🇺🇸 United States

Diagnostix™

DI: 00634782076702 · Model: 5413 · AMERICAN DIAGNOSTIC CORP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Diagnostix™
Primary DI
00634782076702
Version / Model
5413
Catalog Number
5413
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
15c7951e-7b02-4b79-ac1c-5b6bd947bb45

Device Description

Diagnostix Portable Dermascope,3.5v, LED

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
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 00634782578077
Primary 00634782076702

Customer Contacts

Storage Conditions

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