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Everest & Jennings

FDA UDI

Class I (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name
Everest & Jennings FDA UDI
Generic Name
Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible FDA UDI
Device Name
CROSSBRACE 18W - ADJUSTABLE DEPTH &CBOLT-PR (INCLUDES 4 LINKAGES,4 BRACKETS, 2 SADDLE BUSHINGS, 2 GASKETS & HARDWARE) FDA UDI
Model / Reference
907632C2A FDA UDI
Description
CROSSBRACE 18W - ADJUSTABLE DEPTH &CBOLT-PR (INCLUDES 4 LINKAGES,4 BRACKETS, 2 SADDLE BUSHINGS, 2 GASKETS & HARDWARE) FDA UDI

Identifiers

Catalog Number
907632C2A FDA UDI
Primary DI / UDI-DI
M368907632C2A1 FDA UDI
FDA Product Code
KNN FDA UDI
GMDN Term
Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible 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

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: Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible

Everest & Jennings by GF Health Products, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 93af7c13-357a-4b9f-9198-9103b2a2a94f 35 fields · synced May 31, 2026