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Traction frame

FDA UDI

Class II (US FDA UDI)

by Paramount Bed Co., Ltd.

Identity

Trade Name
Traction frame FDA UDI
Generic Name
Bed traction frame FDA UDI
Device Name
Electrical Hospital Bed Accessory to be used for patient traction at medical institutions FDA UDI
Model / Reference
PC-5121 FDA UDI
Description
Electrical Hospital Bed Accessory to be used for patient traction at medical institutions FDA UDI

Identifiers

Primary DI / UDI-DI
04527799701513 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Bed traction frame FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bed traction frame

Traction frame by Paramount Bed Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed traction frame.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82ddd83a-0543-4007-bad7-092df70da0dc 33 fields · synced Jun 1, 2026