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Support Pad

FDA UDI

Class I (US FDA UDI)

by Paramount Bed Co., Ltd.

Identity

Trade Name
Support Pad FDA UDI
Generic Name
Multifunction body cushion FDA UDI
Device Name
Sittan's accessory to support patient abdomen FDA UDI
Model / Reference
KF-80UW FDA UDI
Description
Sittan's accessory to support patient abdomen FDA UDI

Identifiers

Primary DI / UDI-DI
04527799706006 FDA UDI
FDA Product Code
IKX FDA UDI
INW FDA UDI
GMDN Term
Multifunction body cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 FDA UDI
890.3750 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multifunction body cushion

Support Pad by Paramount Bed Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multifunction body cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paramount Bed Co., Ltd.

Sources (1)

  • FDA UDI 30f088d8-00e2-456e-9f1d-ec46a8c3a1f5 33 fields · synced Jun 1, 2026