FDA UDI Not in Commercial Distribution 🇺🇸 United States

Diagnostix™

DI: 00634782076368 · Model: 5630 · AMERICAN DIAGNOSTIC CORP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Diagnostix™
Primary DI
00634782076368
Version / Model
5630
Catalog Number
5630
Company Name
AMERICAN DIAGNOSTIC CORP
Labeler DUNS
108999095
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-17
Public Version
1
Public Version Date
2019-05-27
Public Version Status
New
Public Device Record Key
d50b87e7-aeae-46c3-ae2c-e1c5689aa569
Distribution End Date
2019-05-17

Device Description

Wall Specula Dispenser,

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
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
HLJ Ophthalmoscope, Battery-Powered

GMDN Terms

Code Name
45084 Ophthalmic/otologic diagnostic set

Identifiers

Type ID
Primary 00634782076368

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K950914 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
23 – 122 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
0 – 85 Percent (%) Relative Humidity