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Posey

FDA UDI

Class I (US FDA UDI)

by Posey Products, Llc

Identity

Trade Name
POSEY FDA UDI
Generic Name
Patient-monitoring bed mattress cover FDA UDI
Device Name
POSEY KEEPSAFE DELUXE FDA UDI
Model / Reference
8374 FDA UDI
Description
POSEY KEEPSAFE DELUXE FDA UDI

Identifiers

Catalog Number
1074 FDA UDI
Primary DI / UDI-DI
10190676004888 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Patient-monitoring bed mattress cover FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2400 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient-monitoring bed mattress cover

Posey by Posey Products, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient-monitoring bed mattress cover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Posey Products, Llc

Sources (1)

  • FDA UDI d817fbcc-2fdf-4731-91fc-23c9f79ccf6f 34 fields · synced Jun 8, 2026