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Hill-Rom

FDA UDI

Class II (US FDA UDI)

by Tridien Medical

Identity

Trade Name
Hill-Rom FDA UDI
Generic Name
Rotation bed, electric FDA UDI
Device Name
Controller CAP HV TUR MKS E FDA UDI
Model / Reference
Compella FDA UDI
Description
Controller CAP HV TUR MKS E FDA UDI

Identifiers

Catalog Number
23SM-CHE-TRM-E FDA UDI
Primary DI / UDI-DI
00841965101070 FDA UDI
FDA Product Code
IKZ FDA UDI
GMDN Term
Rotation bed, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5225 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rotation bed, electric

Hill-Rom by Tridien Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rotation bed, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tridien Medical

Sources (1)

  • FDA UDI 351d054b-f94c-431b-bf41-319cbcd5bcaa 35 fields · synced May 30, 2026