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PachPen

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 24-5100

by Accutome Inc. DBA Keeler USA

Identity

Trade Name
PachPen EUDAMEDFDA UDI
Generic Name
Ultrasound pachymeter FDA UDI
Device Name
PachPen EUDAMED
Model / Reference
24-5100 EUDAMEDFDA UDI

Identifiers

Catalog Number
24-5100 FDA UDI
Primary DI / UDI-DI
00897826002017 EUDAMEDFDA UDI
Basic UDI-DI
B-00897826002017 EUDAMED
FDA Product Code
IYO FDA UDI
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
GMDN Term
Ultrasound pachymeter FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
Market of Registration
Germany 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

PachPen 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 f67a690b-43ef-427e-9c1b-5486ae3472ff 61 fields · synced Aug 1, 2026
  • FDA UDI ca8db09f-d072-4385-9efb-086526778535 33 fields · synced May 30, 2026