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Bariatric HD Elevating Leg Rest - 32" WC

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Bariatric HD Elevating Leg Rest (for 26", 28", 30", 32" WC) FDA UDI
Generic Name
Wheelchair footrest/legrest FDA UDI
Model / Reference
10264 FDA UDI

Identifiers

Primary DI / UDI-DI
00616784026411 FDA UDI
FDA Product Code
IMM FDA UDI
GMDN Term
Wheelchair footrest/legrest FDA UDI
Models / Variants
for 26" FDA UDI
28" FDA UDI
30" FDA UDI
32" WC FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wheelchair footrest/legrest

Bariatric HD Elevating Leg Rest - 32" WC by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — 4 models — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair footrest/legrest.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI a0220fb9-a6f0-45f1-9db6-005471613f0d 32 fields · synced May 30, 2026