← Back to catalogue

SIMMONS Clinical Care

FDA UDI

Class II (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name
SIMMONS Clinical Care FDA UDI
Generic Name
Alternating-pressure bed mattress overlay system FDA UDI
Device Name
Clinical Plus Alternating Pressure/Low Air Loss Mattress System FDA UDI
Model / Reference
760000S FDA UDI
Description
Clinical Plus Alternating Pressure/Low Air Loss Mattress System FDA UDI

Identifiers

Primary DI / UDI-DI
M368760000S1 FDA UDI
FDA Product Code
FNM FDA UDI
GMDN Term
Alternating-pressure bed mattress overlay system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5550 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Alternating-pressure bed mattress overlay system

SIMMONS Clinical Care by GF Health Products, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure bed mattress overlay system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
GF Health Products, Inc

Sources (1)

  • FDA UDI 5f1a8f43-77d4-4ab7-88e9-6e1a968bf3ad 35 fields · synced Jun 8, 2026