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Pulsair Intellipuff

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 2414-P-2001

by Keeler Ltd

Identity

Trade Name
Pulsair Intellipuff EUDAMEDFDA UDI
Generic Name
Ophthalmic tonometer, line-powered FDA UDI
Device Name
Pulsair Intellipuff EUDAMED
Model / Reference
2414-P-2001 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
05055272707237 EUDAMEDFDA UDI
Basic UDI-DI
B-05055272707237 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
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

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

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 Intellipuff 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 e5e2ea18-34ca-4825-b467-3df32a9b0886 61 fields · synced Jul 21, 2026
  • FDA UDI a4893682-fde3-4cd9-b5ad-5dcc9c88718a 32 fields · synced May 30, 2026