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Pedal Exerciser, Folding, Digital, Hands/Feet

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Pedal Exerciser, Folding, Digital, Hands/Feet FDA UDI
Generic Name
Bicycle exerciser FDA UDI
Model / Reference
10502 FDA UDI

Identifiers

Primary DI / UDI-DI
00616784050218 FDA UDI
FDA Product Code
ISD FDA UDI
GMDN Term
Bicycle exerciser FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5360 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bicycle exerciser

Pedal Exerciser, Folding, Digital, Hands/Feet by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bicycle exerciser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 59db25a0-8ea6-473c-83af-544737134ca4 32 fields · synced May 30, 2026