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Avalon Fetal & Maternal Patch

FDA UDI

Class II (US FDA UDI)

by Philips Medical Systems Hsg

Identity

Trade Name
Avalon Fetal & Maternal Patch FDA UDI
Generic Name
Foetal/maternal prenatal monitor FDA UDI
Device Name
Avalon CL Fetal & Maternal Patch to be used with Avalon CL Fetal & Maternal Pod 866488. Patch is Single Patient Use and consists of a cradle and 5 electrodes. 1 Box= 10 patches. FDA UDI
Model / Reference
Avalon CL Fetal & Maternal Patch FDA UDI
Description
Avalon CL Fetal & Maternal Patch to be used with Avalon CL Fetal & Maternal Pod 866488. Patch is Single Patient Use and consists of a cradle and 5 electrodes. 1 Box= 10 patches. FDA UDI

Identifiers

Catalog Number
989803196341 FDA UDI
Primary DI / UDI-DI
20884838059324 FDA UDI
FDA Product Code
HFM FDA UDI
GMDN Term
Foetal/maternal prenatal monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2720 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Foetal/maternal prenatal monitor

Avalon Fetal & Maternal Patch by Philips Medical Systems Hsg — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foetal/maternal prenatal monitor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f21853bf-14bf-4e5c-9f8c-969cfc091307 36 fields · synced May 30, 2026