Medi RKIT4106

by Medi Manufacturing, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00636257131350 UDI-DI	Date4 Jan 2019Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Medi
Generic Name: Knee support orthosis
Model / Reference: RKIT4106
Description: M4S REPLACEMENT PAD&STRAP SET XXL RT

Primary DI / UDI-DI: 00636257131350
FDA Product Code: ITQ
GMDN Term: Knee support orthosis

Device Class: Class I
Regulation Number: 890.3475
GUDID distribution status: In Commercial Distribution

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Properties

Single Use
Over-the-Counter
Premarket Exempt
Manufacturing Date

Other properties (10)

Sterile: No
Implantable: No
Contains Latex: No
Prescription Use: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Lot / Batch Number: No
Serial Number: No
Expiration Date: No