FDA UDI In Commercial Distribution 🇺🇸 United States

Sunmed

DI: 10889483042212 · Model: 5-0239-61 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sunmed
Primary DI
10889483042212
Version / Model
5-0239-61
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-29
Public Version
5
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
b5a81a83-889b-4609-8d82-3d792c07e5fe

Device Description

Opthalmoscope Lamp 3.5V

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HLJ Ophthalmoscope, Battery-Powered

GMDN Terms

Code Name
46786 Direct ophthalmoscope

Identifiers

Type ID
Primary 10889483042212

Customer Contacts

Phone
800-433-2797

Premarket Submissions

Submission Number Supplement Number
K131719 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
General Warehouse. Do not get wet.