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Q Assist Bar

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Q Assist Bar FDA UDI
Generic Name
Bedrail FDA UDI
Device Name
Q Assist Bar (Compatible with Dynarex D-Series LTC Beds), 1 Pair FDA UDI
Model / Reference
12952 FDA UDI
Description
Q Assist Bar (Compatible with Dynarex D-Series LTC Beds), 1 Pair FDA UDI

Identifiers

Primary DI / UDI-DI
00616784295213 FDA UDI
FDA Product Code
FNJ FDA UDI
GMDN Term
Bedrail FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5120 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: Bedrail

Q Assist Bar by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedrail.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 9e50da83-b73c-4f3c-bc1c-d90ded2b6e3c 33 fields · synced Jun 6, 2026