← Back to catalogue

Posey

FDA UDI

Class II (US FDA UDI)

by Posey Products, Llc

Identity

Trade Name
POSEY FDA UDI
Generic Name
Bedrail pad FDA UDI
Device Name
TOTAL CARE SEIZURE PADS FDA UDI
Model / Reference
5746 FDA UDI
Description
TOTAL CARE SEIZURE PADS FDA UDI

Identifiers

Catalog Number
5746 FDA UDI
Primary DI / UDI-DI
10190676000248 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Bedrail pad FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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: Bedrail pad

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

Similar devices

Also classified as Bedrail pad.

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
Posey Products, Llc

Sources (1)

  • FDA UDI bfea33ac-60f5-47ac-874a-36128549cc94 34 fields · synced Jun 1, 2026