Identity
- Trade Name
- HASA OPTIX EUDAMEDSterile, Single Use, Lasik Flap Lifter/Elevator Binder, 120mm FDA UDI
- Generic Name
- Ophthalmic curette, single-use FDA UDI
- Device Name
- 554504x10: Sterile, Single Use, Lasik Flap Lifter/Elevator Binder, 120mm EUDAMED
- Model / Reference
- 554504 EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 05404027421537 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05404027421537 EUDAMED
- FDA Product Code
- HND FDA UDI
- EMDN Code
- Q021104 OPHTHALMIC SURGERY MANIPULATORS, SINGLE-USE EUDAMED
- GMDN Term
- Ophthalmic curette, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass 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
Category: Ophthalmic surgical probe, single-use
Hasa Optix by Hasa Optix — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic surgical probe, single-use.
- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
- Epithelial Spatula — BLINK MEDICAL LIMITED · Class I
- S14105 — OPHMED CO., LTD. · Class IIa
- S31264 — OPHMED CO., LTD. · Class IIa
- NUCLEUS Y-HOOK HORIZONTAL 12B — Bausch & Lomb, Inc. · Class I
- Anodyne Surgical — Psi/Eye-Ko, Inc. · Class I
- Ophthalmic Hooks — Katena Products, Inc. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05404027421537 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hasa Optix
- EUDAMED SRN
- BE-MF-000028219
Sources (2)
- EUDAMED 6fc00707-a7e8-425b-b8fa-641a1ce94466 61 fields · synced May 30, 2026
- FDA UDI 9582a39a-659c-429f-a30e-3c627f586454 34 fields · synced May 29, 2026