FDA UDI In Commercial Distribution 🇺🇸 United States

MICOR drive

DI: 00860000122375 · Model: FG-50631 · Carl Zeiss Meditec, Cataract Technology, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MICOR drive
Primary DI
00860000122375
Version / Model
FG-50631
Company Name
Carl Zeiss Meditec, Cataract Technology, Inc.
Labeler DUNS
080125056
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-29
Public Version
2
Public Version Date
2023-04-21
Public Version Status
Update
Public Device Record Key
eed9a2ce-85ed-4070-abde-e97721134193

Device Description

Reusable ophthalmic instrument for the removal of cataracts. Connects to MICOR extractor or MICOR vitrector

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
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HQC Unit, Phacofragmentation

GMDN Terms

Code Name
45071 Phacoemulsification system

Identifiers

Type ID
Package 30860000122376
Primary 00860000122375

Customer Contacts

Phone
925-595-9817

Premarket Submissions

Submission Number Supplement Number
K200584 000