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Dynarex Protech 45-Day Chair Sensor Pad, 10" x 15"

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Dynarex Protech 45-Day Chair Sensor Pad, 10" x 15" FDA UDI
Generic Name
Bed/chair occupant movement pressure/vibration sensor FDA UDI
Model / Reference
P-105500 FDA UDI

Identifiers

Primary DI / UDI-DI
00840117323094 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Bed/chair occupant movement pressure/vibration sensor 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bed/chair occupant movement pressure/vibration sensor

Dynarex Protech 45-Day Chair Sensor Pad, 10" x 15" by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed/chair occupant movement pressure/vibration sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 59230885-8216-46d8-9891-6d3543e60b92 32 fields · synced Jun 6, 2026