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532nm LIO

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 1205-P-2130

by Keeler Ltd

Identity

Trade Name
532nm LIO EUDAMEDFDA UDI
Generic Name
Indirect binocular laser ophthalmoscope FDA UDI
Device Name
532nm LIO EUDAMED
Model / Reference
1205-P-2130 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05055272719674 EUDAMEDFDA UDI
Basic UDI-DI
B-05055272719674 EUDAMED
FDA Product Code
HQF FDA UDI
EMDN Code
Z12120199 OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER EUDAMED
GMDN Term
Indirect binocular laser ophthalmoscope FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
886.4390 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

532nm LIO by Keeler Ltd — Class IIb — 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
Keeler Ltd
EUDAMED SRN
GB-MF-000009031
Authorised Representative
Keeler Europe Distribution, S.L. ES-AR-000001559

Sources (2)

  • EUDAMED a5cf1a24-eeec-4cd2-816e-20c5d78b4dd3 61 fields · synced Jul 21, 2026
  • FDA UDI 9d8c23d6-170e-46b1-9d0d-3629cab2de28 32 fields · synced May 30, 2026