Compass International RU-300

Trade name

Compass International

Generic name

Medical ruler, single-use

Model / Ref / Catalog

RU-300

Primary DI / UDI-DI

B169RU3000

FDA product code

HAW

GMDN term

Medical ruler, single-use

Device class

Class II

Regulation number

882.4560

GUDID distribution status

In Commercial Distribution

Sterilisation method

Ethylene Oxide

Category: Medical ruler, single-use

Other devices filed under FDA product code HAW (Neurological Stereotaxic Instrument).

• NAVIPRO KNEE SOFTWARE MODULE by Kinamed, Inc.
• Vertek® 9733936 by Medtronic Navigation Inc.
• VECTORVISION HIP 3.0 by Brainlab AG
• Synergy Cranial by Medtronic Navigation Inc.
• NEXDRIVE™ MI-2000-00772 by FHC, INC.
• NON-INVASIVE DYNAMIC REFERENCE FRAME (DRF) FOR OPTICAL TRACKING SYSTEM, MODEL OTS by Radionics, Inc.
• 6001-022-000 by Stryker Leibinger
• LEKSELL STEREOTACTIC SYSTEM by Elekta Instrument AB
• ACUMEN IMAGE GUIDED SURGICAL SYSTEM by Ebi, L.P.
• ORTHOPILOT HTO MODULE by AESCULAP, INC.

• COMPASS CYGNUS-PFS IGS System CYG-PFSN-10TP

  Class II

  FDA 510(k) K964229 Active Cleared 19 Aug 1997 GUDID on market

• COMPASS Stereotactic System PION-20

  Class II

  FDA 510(k) K871046 Active Cleared 8 May 1987 GUDID on market

• COMPASS CT Adaptation Stereotactic System PION-20

  Class II

  FDA 510(k) K862220 Active Cleared 18 Jun 1986 GUDID on market

• COMPASS Stereotactic Retractor System PION-20

  Class II

  FDA 510(k) K896156 Active Cleared 6 Dec 1989 GUDID on market

See all devices from Compass International →