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Hasa Optix

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 554055

by Hasa Optix

Identity

Trade Name
HASA OPTIX EUDAMED
Sterile, Single Use, Phaco Chopper, Right Hand, 110mm FDA UDI
Generic Name
Ophthalmic curette, single-use FDA UDI
Device Name
554055x10: Sterile, Single Use, Phaco Chopper, Right Hand, 110mm EUDAMED
Model / Reference
554055 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05404027422480 EUDAMEDFDA UDI
Basic UDI-DI
B-05404027422480 EUDAMED
FDA Product Code
HND FDA UDI
EMDN Code
Q021199 OPHTHALMIC SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
GMDN Term
Ophthalmic curette, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Hasa Optix by Hasa Optix — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hasa Optix
EUDAMED SRN
BE-MF-000028219

Sources (2)

  • EUDAMED c23d5dd2-a4b3-41be-8e5c-bfc7f3bf9942 61 fields · synced May 30, 2026
  • FDA UDI 538a507d-069b-4127-a2c9-50afc5b4c043 34 fields · synced May 30, 2026