micromed SD LTM 32 EXPRESS

by Micromed, Inc.

micromed SD LTM 32 EXPRESS is a Class II device made by Micromed, Inc., cleared under FDA 510(k) K071782 on 10 Jan 2008 and listed in FDA GUDID since 21 Mar 2018 (UDI-DI 08033928120736), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number08033928120736 UDI-DI	Date21 Mar 2018Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Abbreviated	NumberK071782	Date10 Jan 2008Decided	StatusActive

Official records

AccessGUDID record UDI-DI 08033928120736
FDA 510(k) database 510(k) number K071782

Across registries

2 registries list this device

FDA 510(k) K071782 decided 10 Jan 2008 Active
FDA GUDID UDI-DI 08033928120736 listed 21 Mar 2018 Listed

Timeline

2 dated events

10 Jan 2008 Cleared FDA 510(k) K071782
21 Mar 2018 Listed FDA GUDID 08033928120736

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: micromed
Generic name: Patient monitoring system module, electroencephalographic
Model / reference: SD LTM 32 EXPRESS

Primary DI / UDI-DI: 08033928120736
510(k) Number: K071782
FDA product code: OLV
GMDN term: Patient monitoring system module, electroencephalographic

Device class: Class II
Regulation number: 882.1400
GUDID distribution status: In Commercial Distribution

Other devices from Micromed, Inc.

See all devices from Micromed, Inc. →

Properties

Prescription use
Serial number
Manufacturing date

Other properties (12, all answered No)