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chiyuan

FDA UDI

Class I (US FDA UDI)

by Jinan Chiyuan Biotechnology Co., Ltd

Identity

Trade Name
chiyuan FDA UDI
Generic Name
Alternating-pressure chair cushion, reusable FDA UDI
Device Name
Pressure reducing seat cushion FDA UDI
Model / Reference
PL FDA UDI
Description
Pressure reducing seat cushion FDA UDI

Identifiers

Primary DI / UDI-DI
06977197385019 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Alternating-pressure chair cushion, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 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: Alternating-pressure chair cushion, reusable

chiyuan by Jinan Chiyuan Biotechnology Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure chair cushion, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dd6aa6a3-9134-403a-a606-fe8b335f233f 33 fields · synced May 30, 2026