← Back to catalogue

MedX

FDA UDI

Class II (US FDA UDI)

by Medx Holdings, Inc.

Identity

Trade Name
MedX FDA UDI
Generic Name
Core-body mechanical weight exerciser FDA UDI
Device Name
Measuring exercise equipment FDA UDI
Model / Reference
Lumbar FDA UDI
Description
Measuring exercise equipment FDA UDI

Identifiers

Primary DI / UDI-DI
00851688007016 FDA UDI
FDA Product Code
ISD FDA UDI
GMDN Term
Core-body mechanical weight 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Core-body mechanical weight exerciser

MedX by Medx Holdings, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Core-body mechanical weight exerciser.

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

Manufacturer
Medx Holdings, Inc.

Sources (1)

  • FDA UDI ec4b43e5-982a-4747-b021-bfa582d92359 34 fields · synced Jun 8, 2026