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Slz 5xp Di Ref

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 3020-P-2035

by Keeler Ltd

Identity

Trade Name
SLZ 5XP DI REF EUDAMEDFDA UDI
Generic Name
Ophthalmic examination slit lamp FDA UDI
Device Name
Slit Lamp EUDAMED
Model / Reference
3020-P-2035 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05055272715355 EUDAMEDFDA UDI
Basic UDI-DI
50552727SLITLAMPSRG EUDAMED
Direct Marketing DI
05055272715355 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
Spain 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 5xp Di Ref 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 923aab0c-d04c-48dc-b609-b5d3678f6981 61 fields · synced Jul 16, 2026
  • FDA UDI 84f64386-ce3a-4feb-8432-c5f4ab984136 32 fields · synced May 30, 2026