← Back to catalogue

MICOR Auto I/A

FDA UDI

Class II (US FDA UDI)

by Carl Zeiss Meditec Cataract Technology Inc

Identity

Trade Name
MICOR Auto I/A FDA UDI
Generic Name
Phacoemulsification/vitrectomy system FDA UDI
Device Name
MICOR Automatic Irrigation Device FDA UDI
Model / Reference
FG-51820 FDA UDI
Description
MICOR Automatic Irrigation Device FDA UDI

Identifiers

Primary DI / UDI-DI
00850005541080 FDA UDI
510(k) Number
K243395 FDA UDI
FDA Product Code
HQC FDA UDI
MLZ FDA UDI
GMDN Term
Phacoemulsification/vitrectomy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 FDA UDI
886.4150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Phacoemulsification/vitrectomy system

MICOR Auto I/A by Carl Zeiss Meditec Cataract Technology Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phacoemulsification/vitrectomy system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 254f025a-81ab-4c67-a368-a68b62ed118a 35 fields · synced Jun 8, 2026