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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
Low-air-loss bed FDA UDI
Device Name
Controller/Transport/ Excel Ca FDA UDI
Model / Reference
ExcelCare Transport FDA UDI
Description
Controller/Transport/ Excel Ca FDA UDI

Identifiers

Catalog Number
23-SMMIL3TPHR02 FDA UDI
Primary DI / UDI-DI
00841965101209 FDA UDI
FDA Product Code
IKZ FDA UDI
GMDN Term
Low-air-loss bed 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: Low-air-loss bed

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

Similar devices

Also classified as Low-air-loss bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tridien Medical

Sources (1)

  • FDA UDI aa279f5c-3815-485a-a582-83092e03d2c7 35 fields · synced May 30, 2026