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Hasa Optix

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref HA-SET008

by Hasa Optix

Identity

Trade Name
HASA OPTIX EUDAMED
Rayner Cataract Set 8 FDA UDI
Generic Name
Ophthalmic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
HA-SET008: Sterile, Single Use, CATARACT SET RAYNER 8 EUDAMED
Model / Reference
HA-SET008 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05404027444567 EUDAMEDFDA UDI
Basic UDI-DI
B-05404027444567 EUDAMED
FDA Product Code
PZG FDA UDI
EMDN Code
Q021113 OPHTHALMIC SURGERY INSTRUMENT KITS, SINGLE-USE EUDAMED
GMDN Term
Ophthalmic surgical procedure kit, non-medicated, 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

Yes

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 af1588b9-be3d-4342-82ea-9ceb1ff3b57f 61 fields · synced May 30, 2026
  • FDA UDI 9d98f5a9-4243-4900-a24c-8698cfd148a3 34 fields · synced May 30, 2026