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Reusable phaco sleeve 2.2 mm

FDA UDI

Class II (US FDA UDI)

by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

Identity

Trade Name
Reusable phaco sleeve 2.2 mm FDA UDI
Generic Name
Phacoemulsification system handpiece FDA UDI
Model / Reference
3009.IR22 FDA UDI

Identifiers

Catalog Number
3009.IR22 FDA UDI
Primary DI / UDI-DI
08717872030371 FDA UDI
510(k) Number
K190875 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Phacoemulsification system handpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Phacoemulsification system handpiece

Reusable phaco sleeve 2.2 mm by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Phacoemulsification system handpiece.

Cleared under the same submission

K190875 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI befb7762-eb00-4a2f-8916-823d98b50859 34 fields · synced May 30, 2026