OAR 332-026-0030: Approved Devices

Edition: Current OARD snapshotEffective: 2020-01-01Last verified: 2026-09-07

An LDM may use the following Board approved devices: (1) Devices for injection of medications including: (a) Needles. (b) Syringes. (2) Devices for administration of intravenous fluids including: (a) Drip sets. (b) Catheters. (3) Devices for maternal and neonatal resuscitation including: (a) Suction devices; (b) Oxygen-delivery devices. (c) Bag-Valve-Mask-Sets. (4) Devices for rupturing the amniotic sac. (5) Devices for repairing the perineal area including: (a) Sutures; (b) Instruments for completing a repair. (c) Local anesthetic administration devices.

Official history and status

Statutory/Other Authority: ORS 676.615 & ORS 687.493

Statutes/Other Implemented: ORS 687.493

History: DEM 3-2019, amend filed 12/19/2019, effective 01/01/2020 Renumbered from 332-025-0060 by DEM 5-2011, f. & cert. ef. 9-26-11 DEM 6-2010, f. 12-30-10, cert. ef. 1-1-11 DEM 1-2002, f. 2-25-02 cert. ef. 3-1-02 DEM 1-2001(Temp), f. & cert. ef. 10-1-01 thru 3-29-02

This rule cites

No citations extracted.

Cited by

OAR 332-026-0000: Access to and Administration of Legend Drugs and Devices

Official source: https://secure.sos.state.or.us/oard/