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Dr-Hos

FDA UDI

Class I (US FDA UDI)

by Guangzhou Xinbo Electronic Co., Ltd.

Identity

Trade Name
DR-HOS FDA UDI
Generic Name
Bed pillow, reusable FDA UDI
Device Name
Adjustable Pillow – Queen size FDA UDI
Model / Reference
DHP-Queen FDA UDI
Description
Adjustable Pillow – Queen size FDA UDI

Identifiers

Primary DI / UDI-DI
06970742220285 FDA UDI
FDA Product Code
IQK FDA UDI
GMDN Term
Bed pillow, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3490 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
MRI Safety
MR Unsafe FDA UDI

Category: Bed pillow, reusable

Dr-Hos by Guangzhou Xinbo Electronic Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed pillow, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fd272195-0498-41db-9c74-6a81caf4441e 33 fields · synced Jun 8, 2026