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Slz 3xc Tbl

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 3020-P-2042

by Keeler Ltd

Identity

Trade Name
SLZ 3XC TBL EUDAMEDFDA UDI
Generic Name
Ophthalmic examination slit lamp FDA UDI
Device Name
Slit Lamp EUDAMED
Model / Reference
3020-P-2042 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05055272715423 EUDAMEDFDA UDI
Basic UDI-DI
50552727SLITLAMPSRG EUDAMED
Direct Marketing DI
05055272715423 EUDAMED
FDA Product Code
HJO FDA UDI
EMDN Code
Z12120108 SLIT LAMPS EUDAMED
GMDN Term
Ophthalmic examination slit lamp FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
886.1850 FDA UDI
Market of Registration
Latvia 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

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

Slz 3xc Tbl by Keeler Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

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 fd64b791-cab6-4f38-b015-4e8e3309cbe1 61 fields · synced Jul 15, 2026
  • FDA UDI d04e1bf9-afc9-4054-8e3b-aac83a9e5f69 32 fields · synced May 30, 2026