← Back to catalogue

Hhp, 103, 8, Up/Dn Arrows, Kenall

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
HHP,103,8,UP/DN ARROWS,KENALL FDA UDI
Generic Name
Pillow speaker FDA UDI
Device Name
HHP,103,8,UP/DN ARROWS,KENALL FDA UDI
Model / Reference
C-3412 FDA UDI
Description
HHP,103,8,UP/DN ARROWS,KENALL FDA UDI

Identifiers

Catalog Number
4143 FDA UDI
Primary DI / UDI-DI
00840828149914 FDA UDI
FDA Product Code
IQA FDA UDI
GMDN Term
Pillow speaker FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3725 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pillow speaker

Hhp, 103, 8, Up/Dn Arrows, Kenall by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pillow speaker.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Curbell Medical Products, Inc.

Sources (1)

  • FDA UDI 1cf91860-a336-4582-b220-eead8b8bd51c 35 fields · synced Jun 1, 2026