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AccuPen

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 24-3000

by Accutome Inc. DBA Keeler USA

Identity

Trade Name
AccuPen EUDAMEDFDA UDI
Generic Name
Ophthalmic tonometer, battery-operated FDA UDI
Device Name
AccuPen EUDAMED
Model / Reference
24-3000 EUDAMEDFDA UDI

Identifiers

Catalog Number
24-3000 FDA UDI
Primary DI / UDI-DI
00897826002000 EUDAMEDFDA UDI
Basic UDI-DI
B-00897826002000 EUDAMED
FDA Product Code
HKY FDA UDI
EMDN Code
Z12120122 TONOMETERS EUDAMED
GMDN Term
Ophthalmic tonometer, battery-operated FDA UDI

Classification

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

Yes

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

AccuPen by Accutome Inc. DBA Keeler USA — 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

EUDAMED SRN
US-MF-000036181
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED e33a6399-04d6-4070-840a-440fa3384438 61 fields · synced Jul 9, 2026
  • FDA UDI 0f7a7d23-1ae1-4ab3-a927-2fb37612b2bd 33 fields · synced May 30, 2026