Stet Cube 1

by Light Progress SRL

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	Number08052780880312 UDI-DI	Date12 Sep 2017Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Stet Cube
Generic Name: Ultraviolet stethoscope disinfector
Model / Reference: 1

Primary DI / UDI-DI: 08052780880312
FDA Product Code: MEC
GMDN Term: Ultraviolet stethoscope disinfector

Device Class: Class II
Regulation Number: 880.6992
GUDID distribution status: In Commercial Distribution

Other devices from Light Progress SRL

Stet Clean 1

Class II

Properties

Premarket Exempt
Lot / Batch Number
Serial Number
Manufacturing Date

Other properties (10)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Expiration Date: No