← Back to catalogue

0900, R5, Std, 1 Lt, Av

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
0900,R5,STD,1 LT,AV FDA UDI
Generic Name
Pillow speaker FDA UDI
Device Name
0900,R5,STD,1 LT,AV FDA UDI
Model / Reference
350226 FDA UDI
Description
0900,R5,STD,1 LT,AV FDA UDI

Identifiers

Catalog Number
614 FDA UDI
Primary DI / UDI-DI
00840828101202 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

A comprehensive medical device directory listing the 0900, R5, STD, 1 LT, AV pillow speaker for relaxation, entertainment, and sleep improvement.

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 7f021e42-a2c9-4de8-b184-5c7a1bc54830 35 fields · synced Jul 31, 2026