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Pulsair Desktop

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 2417-P-2000

by Keeler Ltd

Identity

Trade Name
Pulsair Desktop EUDAMED
Pulsair Desktop (complete) FDA UDI
Generic Name
Ophthalmic tonometer, line-powered FDA UDI
Device Name
Pulsair Desktop EUDAMED
Model / Reference
2417-P-2000 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05055272711746 EUDAMEDFDA UDI
Basic UDI-DI
B-05055272711746 EUDAMED
FDA Product Code
HKX FDA UDI
EMDN Code
Z12120122 TONOMETERS EUDAMED
GMDN Term
Ophthalmic tonometer, line-powered FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
886.1930 FDA UDI
Market of Registration
Sweden 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

Yes

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

Pulsair Desktop by Keeler Ltd — 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
Keeler Ltd
EUDAMED SRN
GB-MF-000009031
Authorised Representative
Keeler Europe Distribution, S.L. ES-AR-000001559

Sources (2)

  • EUDAMED 31b889da-680b-4f4c-b52b-274d6b483632 61 fields · synced May 30, 2026
  • FDA UDI f22a7249-3a64-4577-a124-078e9067e6e7 32 fields · synced May 30, 2026