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Sonicaid

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 8400-6919Model ACC-OBS-008

by ArjoHuntleigh AB

Identity

Trade Name
SONICAID EUDAMEDFDA UDI
Generic Name
Foetal Doppler system probe FDA UDI
Device Name
1MHz ULTRASOUND TRANSDUCER (2m) EUDAMED
1.5Mhz ULTRASOUND TRANSDUCER FDA UDI
Model / Reference
ACC-OBS-008 EUDAMED
8400-6919 EUDAMEDFDA UDI
Description
1.5Mhz ULTRASOUND TRANSDUCER FDA UDI

Identifiers

Catalog Number
8400-6919 FDA UDI
Primary DI / UDI-DI
05051968008237 EUDAMEDFDA UDI
Basic UDI-DI
5060693520440W7 EUDAMED
510(k) Number
K912639 FDA UDI
FDA Product Code
HGM FDA UDI
EMDN Code
Z1104018099 ULTRASOUND SCANNERS – HARDWARE ACCESSORIES – OTHER EUDAMED
GMDN Term
Foetal Doppler system probe FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
884.2740 FDA UDI
Market of Registration
Ireland 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

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

Sonicaid by Arjohuntleigh AB — 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
ArjoHuntleigh AB
EUDAMED SRN
SE-MF-000000696

Sources (2)

  • EUDAMED 81ae624e-c873-45ca-ace0-9e0042d323d7 61 fields · synced Jun 19, 2026
  • FDA UDI 269a7c10-8a75-4d41-81bd-a42218c014f8 37 fields · synced May 30, 2026