← Back to catalogue

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
W/C TRAV L3 PLUS 16X16 FLIP-BACK DESK ARM, D-FTR E&J FDA UDI
Model / Reference
3F012220 FDA UDI
Description
W/C TRAV L3 PLUS 16X16 FLIP-BACK DESK ARM, D-FTR E&J FDA UDI

Identifiers

Catalog Number
3F012220 FDA UDI
Primary DI / UDI-DI
M3683F0122201 FDA UDI
510(k) Number
K082784 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3850 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

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.

Cleared under the same submission

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

Sources (1)

  • FDA UDI e6634fac-5317-4a15-8c50-a2a99cdb30c1 36 fields · synced May 30, 2026