FDA UDI In Commercial Distribution 🇺🇸 United States

ZEISS

DI: 03664188000589 · Model: VISUREF 1000 · LUNEAU TECHNOLOGY OPERATIONS
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ZEISS
Primary DI
03664188000589
Version / Model
VISUREF 1000
Company Name
LUNEAU TECHNOLOGY OPERATIONS
Labeler DUNS
260432380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-11
Public Version
1
Public Version Date
2025-03-19
Public Version Status
New
Public Device Record Key
1320e0dc-d0c8-4ebc-a10c-e17407d40ff6

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HKI Camera, Ophthalmic, Ac-Powered
HKX Tonometer, Ac-Powered

GMDN Terms

Code Name
10551 Ophthalmic fundus camera
65176 Multiple ocular dimension meter

Identifiers

Type ID
Primary 03664188000589