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20G Disposable phaco fragmentation needle, incl. wrench

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
20G Disposable phaco fragmentation needle, incl. wrench FDA UDI
Generic Name
Phacoemulsification system handpiece tip, single-use FDA UDI
Model / Reference
8400.FT FDA UDI

Identifiers

Primary DI / UDI-DI
08717872033044 FDA UDI
510(k) Number
K190875 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Phacoemulsification system handpiece tip, single-use 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

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Phacoemulsification system handpiece tip, single-use

20G Disposable phaco fragmentation needle, incl. wrench by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. — Class II — FDA UDI — listed in FDA…

Similar devices

Also classified as Phacoemulsification system handpiece tip, single-use.

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 7528dccc-3a68-4d7f-9cb7-c86f2796d2e7 33 fields · synced Jun 8, 2026