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Stretcher Surface

FDA UDI

Class II (US FDA UDI)

by Hill-Rom de México, S. de R.L. de C.V.

Identity

Trade Name
Stretcher Surface FDA UDI
Generic Name
Basic bed mattress FDA UDI
Device Name
Hospital Bed Surface FDA UDI
Model / Reference
P1435EC FDA UDI
Description
Hospital Bed Surface FDA UDI

Identifiers

Primary DI / UDI-DI
00887761999244 FDA UDI
FDA Product Code
FPO FDA UDI
GMDN Term
Basic bed mattress FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6910 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Basic bed mattress

Stretcher Surface by Hill-Rom de México, S. de R.L. de C.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic bed mattress.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6d93841f-03eb-4520-be3e-babe72968290 34 fields · synced Jun 1, 2026